curl -X POST https://win.oneshotagent.com/v1/tools/lookup/company-fda-registration \
-H "Content-Type: application/json" \
-H "payment-signature: <base64 x402 payment>" \
-d '{
"registration_number": "1030489"
}'
const response = await fetch("https://win.oneshotagent.com/v1/tools/lookup/company-fda-registration", {
method: "POST",
headers: {
"Content-Type": "application/json",
"payment-signature": paymentProof,
},
body: JSON.stringify({
"registration_number": "1030489"
}),
});
const result = await agent.tool('lookup/company-fda-registration', {
registration_number: '1030489'
});
console.log(result.result);
console.log(result.evidence);
{
"success": true,
"data": {
"request_id": "uuid",
"receipt_id": "rcpt_...",
"status": "completed",
"tool": "company_fda_registration",
"result": {
"total_listings": 533,
"truncated": true,
"establishments": [
{
"registration_number": "1030489",
"fei_number": "1000477302",
"name": "MEDTRONIC SOFAMOR DANEK USA, INC.",
"address": {
"street": "1800 PYRAMID PLACE",
"city": "Memphis",
"state": "TN",
"postal_code": "38132",
"country": "US"
},
"registration_year": 2026,
"active": true,
"initial_importer": true,
"owner_operator": {
"number": "2112641",
"firm_name": "Medtronic, Inc.",
"city": "Minneapolis",
"state": "MN",
"country": "US"
},
"activities": [
"Develop Specifications But Do Not Manufacture At This Facility"
],
"products": [
{
"product_code": "MAX",
"device_name": "Intervertebral Fusion Device With Bone Graft, Lumbar",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K253011",
"proprietary_names": [
"Catalyft PL Expandable Interbody System"
]
},
{
"product_code": "NKB",
"device_name": "Thoracolumbosacral Pedicle Screw System",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "KWP",
"device_name": "Appliance, Fixation, Spinal Interlaminal",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3050",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "KWQ",
"device_name": "Appliance, Fixation, Spinal Intervertebral Body",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3060",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "NKG",
"device_name": "Posterior Cervical Screw System",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3075",
"clearance": "K254165",
"proprietary_names": [
"INFINITY Occipitocervical Upper Thoracic System"
]
},
{
"product_code": "OLO",
"device_name": "Orthopedic Stereotaxic Instrument",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.4560",
"clearance": "K254165",
"proprietary_names": [
"INFINITY Occipitocervical Upper Thoracic System"
]
},
{
"product_code": "OVD",
"device_name": "Intervertebral Fusion Device With Integrated Fixation, Lumbar",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K241992",
"proprietary_names": [
"Catalyft LS Expandable Interbody System"
]
},
{
"product_code": "OSH",
"device_name": "Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "MNH",
"device_name": "Orthosis, Spondylolisthesis Spinal Fixation",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "MNI",
"device_name": "Orthosis, Spinal Pedicle Fixation",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "HBE",
"device_name": "Drills, Burrs, Trephines & Accessories (Simple, Powered)",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.4310",
"clearance": "K210637",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System"
]
},
{
"product_code": "NQP",
"device_name": "Posterior Metal/Polymer Spinal System, Fusion",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": "K191066",
"proprietary_names": [
"CD Horizon Astute Spinal System"
]
},
{
"product_code": "ODP",
"device_name": "Intervertebral Fusion Device With Bone Graft, Cervical",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K153438",
"proprietary_names": [
"PERIMETER® C"
]
},
{
"product_code": "MQP",
"device_name": "Spinal Vertebral Body Replacement Device",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3060",
"clearance": "K131888",
"proprietary_names": [
"T2 XVBR"
]
},
{
"product_code": "NPM",
"device_name": "Bone Grafting Material, Animal Source",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K140374",
"proprietary_names": [
"MASTERGRAFT Putty"
]
},
{
"product_code": "LYC",
"device_name": "Bone Grafting Material, Synthetic",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K140374",
"proprietary_names": [
"MASTERGRAFT Putty"
]
},
{
"product_code": "OVE",
"device_name": "Intervertebral Fusion Device With Integrated Fixation, Cervical",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K142940",
"proprietary_names": [
"Endoskeleton TCS System"
]
},
{
"product_code": "MQV",
"device_name": "Filler, Bone Void, Calcium Compound",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3045",
"clearance": "K130335",
"proprietary_names": [
"Mastergraft ( UltraMatrix, Matrix EXT)"
]
},
{
"product_code": "HWE",
"device_name": "Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment",
"device_class": "1",
"medical_specialty": "General, Plastic Surgery",
"regulation_number": "878.4820",
"clearance": "K123270",
"proprietary_names": [
"POWEREASE System Working Ends"
]
},
{
"product_code": "GWF",
"device_name": "Stimulator, Electrical, Evoked Response",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.1870",
"clearance": "K123270",
"proprietary_names": [
"POWEREASE System Working Ends"
]
},
{
"product_code": "NUN",
"device_name": "Bone Grafting Material, Human Source",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K051188",
"proprietary_names": [
"Grafton DBM"
]
},
{
"product_code": "HRX",
"device_name": "Arthroscope",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.1100",
"clearance": "K103231",
"proprietary_names": [
"Kyphon Inflation Syringe"
]
},
{
"product_code": "HXG",
"device_name": "Tamp",
"device_class": "1",
"medical_specialty": "Orthopedic",
"regulation_number": "888.4540",
"clearance": "K103231",
"proprietary_names": [
"Kyphon Inflation Syringe"
]
},
{
"product_code": "NEK",
"device_name": "Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction",
"device_class": "3",
"medical_specialty": "Unknown",
"regulation_number": null,
"clearance": "P000058",
"proprietary_names": [
"INFUSE BONEGRAFT/ LT-CAGE Lumbar TF"
]
},
{
"product_code": "NQO",
"device_name": "Prosthesis, Spinous Process Spacer/Plate",
"device_class": "3",
"medical_specialty": "Unknown",
"regulation_number": null,
"clearance": "P040001",
"proprietary_names": [
"X-STOP® Interspinous Spacer Titanium"
]
}
]
}
]
},
"evidence": {
"source": "US Food and Drug Administration",
"source_kind": "public",
"retrieved_at": "2026-10-21T00:00:00.000Z",
"calls": [
{
"retrieved_at": "2026-10-21T00:00:00.000Z"
}
],
"as_of": "2026-10-12"
}
}
}
Health
FDA Establishment Registration
Look up medical device establishments, their registration status, activities and listed devices.
POST
/
v1
/
tools
/
lookup
/
company-fda-registration
curl -X POST https://win.oneshotagent.com/v1/tools/lookup/company-fda-registration \
-H "Content-Type: application/json" \
-H "payment-signature: <base64 x402 payment>" \
-d '{
"registration_number": "1030489"
}'
const response = await fetch("https://win.oneshotagent.com/v1/tools/lookup/company-fda-registration", {
method: "POST",
headers: {
"Content-Type": "application/json",
"payment-signature": paymentProof,
},
body: JSON.stringify({
"registration_number": "1030489"
}),
});
const result = await agent.tool('lookup/company-fda-registration', {
registration_number: '1030489'
});
console.log(result.result);
console.log(result.evidence);
{
"success": true,
"data": {
"request_id": "uuid",
"receipt_id": "rcpt_...",
"status": "completed",
"tool": "company_fda_registration",
"result": {
"total_listings": 533,
"truncated": true,
"establishments": [
{
"registration_number": "1030489",
"fei_number": "1000477302",
"name": "MEDTRONIC SOFAMOR DANEK USA, INC.",
"address": {
"street": "1800 PYRAMID PLACE",
"city": "Memphis",
"state": "TN",
"postal_code": "38132",
"country": "US"
},
"registration_year": 2026,
"active": true,
"initial_importer": true,
"owner_operator": {
"number": "2112641",
"firm_name": "Medtronic, Inc.",
"city": "Minneapolis",
"state": "MN",
"country": "US"
},
"activities": [
"Develop Specifications But Do Not Manufacture At This Facility"
],
"products": [
{
"product_code": "MAX",
"device_name": "Intervertebral Fusion Device With Bone Graft, Lumbar",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K253011",
"proprietary_names": [
"Catalyft PL Expandable Interbody System"
]
},
{
"product_code": "NKB",
"device_name": "Thoracolumbosacral Pedicle Screw System",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "KWP",
"device_name": "Appliance, Fixation, Spinal Interlaminal",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3050",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "KWQ",
"device_name": "Appliance, Fixation, Spinal Intervertebral Body",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3060",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "NKG",
"device_name": "Posterior Cervical Screw System",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3075",
"clearance": "K254165",
"proprietary_names": [
"INFINITY Occipitocervical Upper Thoracic System"
]
},
{
"product_code": "OLO",
"device_name": "Orthopedic Stereotaxic Instrument",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.4560",
"clearance": "K254165",
"proprietary_names": [
"INFINITY Occipitocervical Upper Thoracic System"
]
},
{
"product_code": "OVD",
"device_name": "Intervertebral Fusion Device With Integrated Fixation, Lumbar",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K241992",
"proprietary_names": [
"Catalyft LS Expandable Interbody System"
]
},
{
"product_code": "OSH",
"device_name": "Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "MNH",
"device_name": "Orthosis, Spondylolisthesis Spinal Fixation",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "MNI",
"device_name": "Orthosis, Spinal Pedicle Fixation",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "HBE",
"device_name": "Drills, Burrs, Trephines & Accessories (Simple, Powered)",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.4310",
"clearance": "K210637",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System"
]
},
{
"product_code": "NQP",
"device_name": "Posterior Metal/Polymer Spinal System, Fusion",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": "K191066",
"proprietary_names": [
"CD Horizon Astute Spinal System"
]
},
{
"product_code": "ODP",
"device_name": "Intervertebral Fusion Device With Bone Graft, Cervical",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K153438",
"proprietary_names": [
"PERIMETER® C"
]
},
{
"product_code": "MQP",
"device_name": "Spinal Vertebral Body Replacement Device",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3060",
"clearance": "K131888",
"proprietary_names": [
"T2 XVBR"
]
},
{
"product_code": "NPM",
"device_name": "Bone Grafting Material, Animal Source",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K140374",
"proprietary_names": [
"MASTERGRAFT Putty"
]
},
{
"product_code": "LYC",
"device_name": "Bone Grafting Material, Synthetic",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K140374",
"proprietary_names": [
"MASTERGRAFT Putty"
]
},
{
"product_code": "OVE",
"device_name": "Intervertebral Fusion Device With Integrated Fixation, Cervical",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K142940",
"proprietary_names": [
"Endoskeleton TCS System"
]
},
{
"product_code": "MQV",
"device_name": "Filler, Bone Void, Calcium Compound",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3045",
"clearance": "K130335",
"proprietary_names": [
"Mastergraft ( UltraMatrix, Matrix EXT)"
]
},
{
"product_code": "HWE",
"device_name": "Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment",
"device_class": "1",
"medical_specialty": "General, Plastic Surgery",
"regulation_number": "878.4820",
"clearance": "K123270",
"proprietary_names": [
"POWEREASE System Working Ends"
]
},
{
"product_code": "GWF",
"device_name": "Stimulator, Electrical, Evoked Response",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.1870",
"clearance": "K123270",
"proprietary_names": [
"POWEREASE System Working Ends"
]
},
{
"product_code": "NUN",
"device_name": "Bone Grafting Material, Human Source",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K051188",
"proprietary_names": [
"Grafton DBM"
]
},
{
"product_code": "HRX",
"device_name": "Arthroscope",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.1100",
"clearance": "K103231",
"proprietary_names": [
"Kyphon Inflation Syringe"
]
},
{
"product_code": "HXG",
"device_name": "Tamp",
"device_class": "1",
"medical_specialty": "Orthopedic",
"regulation_number": "888.4540",
"clearance": "K103231",
"proprietary_names": [
"Kyphon Inflation Syringe"
]
},
{
"product_code": "NEK",
"device_name": "Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction",
"device_class": "3",
"medical_specialty": "Unknown",
"regulation_number": null,
"clearance": "P000058",
"proprietary_names": [
"INFUSE BONEGRAFT/ LT-CAGE Lumbar TF"
]
},
{
"product_code": "NQO",
"device_name": "Prosthesis, Spinous Process Spacer/Plate",
"device_class": "3",
"medical_specialty": "Unknown",
"regulation_number": null,
"clearance": "P040001",
"proprietary_names": [
"X-STOP® Interspinous Spacer Titanium"
]
}
]
}
]
},
"evidence": {
"source": "US Food and Drug Administration",
"source_kind": "public",
"retrieved_at": "2026-10-21T00:00:00.000Z",
"calls": [
{
"retrieved_at": "2026-10-21T00:00:00.000Z"
}
],
"as_of": "2026-10-12"
}
}
}
Covers medical device establishments registered with the US Food and Drug Administration, worldwide. Supply exactly one registration number, FEI number or firm name. A name search may match many establishments of one group; country narrows name searches only. registration_year is the year the registration runs to. Groups up to 100 source listings into establishments, in first-seen order. Products are unique by product code, at most 25 per establishment, newest created date first; duplicate codes use the newest listing’s details. When truncated is true, only the first 100 source listings are considered: product lists may be incomplete, and name searches may omit entire establishments. Named contacts are excluded. No match returns an empty list. The source refreshes weekly; the evidence date identifies its snapshot.
Authentication
Requires x402 payment in thepayment-signature header.
Request Body
string
The establishment’s FDA registration number.
string
The FDA establishment identifier.
string
Firm name phrase; only letters, digits, spaces, ampersands, hyphens, periods and commas are kept. 2 to 100 characters.
string
Two-letter ISO country code; narrows firm name searches only.
integer
The most establishments to return. From 1 to 10. Defaults to
3.Response (200 OK)
Top-level envelope:success (boolean) and data (object). All fields below are nested under data.
string
Durable job ID for audit and lookup
string
Job status:
completedstring
Always
company_fda_registrationobject
The answer, described under Result below
object
Where the answer came from and when
string
The public body the data comes from. Always
US Food and Drug Administration.string
public when the data comes from a public body, commercial otherwisestring
When the lookup was made, as an ISO 8601 UTC time
string
When the source says the fact was last updated, or
null when the source gives no dateResult
Nested underdata.result.
integer
Total matching source listings, including those beyond the first 100.
boolean
More than 100 source listings matched; only the first 100 are considered, so product lists may be incomplete and name searches may omit entire establishments.
object[]
Matching establishments in first-seen order.
string
Registration number.
string
The FDA Establishment Identifier (FEI).
null when the source gives no value.string
Name.
null when the source gives no value.object
Address.
string
Street.
null when the source gives no value.string
City.
null when the source gives no value.string
State.
null when the source gives no value.string
Postal code.
null when the source gives no value.string
Country.
null when the source gives no value.integer
The year the registration runs to; null when absent.
boolean
Active.
boolean
Initial importer.
object
The establishment’s owner-operator.
string
Number.
null when the source gives no value.string
Firm name.
null when the source gives no value.string
City.
null when the source gives no value.string
State.
null when the source gives no value.string
Country.
null when the source gives no value.string[]
Unique establishment activities across the returned listings.
object[]
Unique product codes, newest listing first, at most 25.
string
Product code.
null when the source gives no value.string
Device name.
null when the source gives no value.string
Device class.
null when the source gives no value.string
Medical specialty.
null when the source gives no value.string
Regulation number.
null when the source gives no value.string
The listing’s clearance or premarket approval number, when present.
null when the source gives no value.string[]
Proprietary names.
curl -X POST https://win.oneshotagent.com/v1/tools/lookup/company-fda-registration \
-H "Content-Type: application/json" \
-H "payment-signature: <base64 x402 payment>" \
-d '{
"registration_number": "1030489"
}'
const response = await fetch("https://win.oneshotagent.com/v1/tools/lookup/company-fda-registration", {
method: "POST",
headers: {
"Content-Type": "application/json",
"payment-signature": paymentProof,
},
body: JSON.stringify({
"registration_number": "1030489"
}),
});
const result = await agent.tool('lookup/company-fda-registration', {
registration_number: '1030489'
});
console.log(result.result);
console.log(result.evidence);
{
"success": true,
"data": {
"request_id": "uuid",
"receipt_id": "rcpt_...",
"status": "completed",
"tool": "company_fda_registration",
"result": {
"total_listings": 533,
"truncated": true,
"establishments": [
{
"registration_number": "1030489",
"fei_number": "1000477302",
"name": "MEDTRONIC SOFAMOR DANEK USA, INC.",
"address": {
"street": "1800 PYRAMID PLACE",
"city": "Memphis",
"state": "TN",
"postal_code": "38132",
"country": "US"
},
"registration_year": 2026,
"active": true,
"initial_importer": true,
"owner_operator": {
"number": "2112641",
"firm_name": "Medtronic, Inc.",
"city": "Minneapolis",
"state": "MN",
"country": "US"
},
"activities": [
"Develop Specifications But Do Not Manufacture At This Facility"
],
"products": [
{
"product_code": "MAX",
"device_name": "Intervertebral Fusion Device With Bone Graft, Lumbar",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K253011",
"proprietary_names": [
"Catalyft PL Expandable Interbody System"
]
},
{
"product_code": "NKB",
"device_name": "Thoracolumbosacral Pedicle Screw System",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "KWP",
"device_name": "Appliance, Fixation, Spinal Interlaminal",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3050",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "KWQ",
"device_name": "Appliance, Fixation, Spinal Intervertebral Body",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3060",
"clearance": "K260216",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System",
"CD Horizon ModuLeX Fenestrated Screw Set"
]
},
{
"product_code": "NKG",
"device_name": "Posterior Cervical Screw System",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3075",
"clearance": "K254165",
"proprietary_names": [
"INFINITY Occipitocervical Upper Thoracic System"
]
},
{
"product_code": "OLO",
"device_name": "Orthopedic Stereotaxic Instrument",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.4560",
"clearance": "K254165",
"proprietary_names": [
"INFINITY Occipitocervical Upper Thoracic System"
]
},
{
"product_code": "OVD",
"device_name": "Intervertebral Fusion Device With Integrated Fixation, Lumbar",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K241992",
"proprietary_names": [
"Catalyft LS Expandable Interbody System"
]
},
{
"product_code": "OSH",
"device_name": "Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "MNH",
"device_name": "Orthosis, Spondylolisthesis Spinal Fixation",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "MNI",
"device_name": "Orthosis, Spinal Pedicle Fixation",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": null,
"proprietary_names": [
"Spinal System"
]
},
{
"product_code": "HBE",
"device_name": "Drills, Burrs, Trephines & Accessories (Simple, Powered)",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.4310",
"clearance": "K210637",
"proprietary_names": [
"CD Horizon ModuLeX Spinal System"
]
},
{
"product_code": "NQP",
"device_name": "Posterior Metal/Polymer Spinal System, Fusion",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3070",
"clearance": "K191066",
"proprietary_names": [
"CD Horizon Astute Spinal System"
]
},
{
"product_code": "ODP",
"device_name": "Intervertebral Fusion Device With Bone Graft, Cervical",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K153438",
"proprietary_names": [
"PERIMETER® C"
]
},
{
"product_code": "MQP",
"device_name": "Spinal Vertebral Body Replacement Device",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3060",
"clearance": "K131888",
"proprietary_names": [
"T2 XVBR"
]
},
{
"product_code": "NPM",
"device_name": "Bone Grafting Material, Animal Source",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K140374",
"proprietary_names": [
"MASTERGRAFT Putty"
]
},
{
"product_code": "LYC",
"device_name": "Bone Grafting Material, Synthetic",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K140374",
"proprietary_names": [
"MASTERGRAFT Putty"
]
},
{
"product_code": "OVE",
"device_name": "Intervertebral Fusion Device With Integrated Fixation, Cervical",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3080",
"clearance": "K142940",
"proprietary_names": [
"Endoskeleton TCS System"
]
},
{
"product_code": "MQV",
"device_name": "Filler, Bone Void, Calcium Compound",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.3045",
"clearance": "K130335",
"proprietary_names": [
"Mastergraft ( UltraMatrix, Matrix EXT)"
]
},
{
"product_code": "HWE",
"device_name": "Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment",
"device_class": "1",
"medical_specialty": "General, Plastic Surgery",
"regulation_number": "878.4820",
"clearance": "K123270",
"proprietary_names": [
"POWEREASE System Working Ends"
]
},
{
"product_code": "GWF",
"device_name": "Stimulator, Electrical, Evoked Response",
"device_class": "2",
"medical_specialty": "Neurology",
"regulation_number": "882.1870",
"clearance": "K123270",
"proprietary_names": [
"POWEREASE System Working Ends"
]
},
{
"product_code": "NUN",
"device_name": "Bone Grafting Material, Human Source",
"device_class": "2",
"medical_specialty": "Dental",
"regulation_number": "872.3930",
"clearance": "K051188",
"proprietary_names": [
"Grafton DBM"
]
},
{
"product_code": "HRX",
"device_name": "Arthroscope",
"device_class": "2",
"medical_specialty": "Orthopedic",
"regulation_number": "888.1100",
"clearance": "K103231",
"proprietary_names": [
"Kyphon Inflation Syringe"
]
},
{
"product_code": "HXG",
"device_name": "Tamp",
"device_class": "1",
"medical_specialty": "Orthopedic",
"regulation_number": "888.4540",
"clearance": "K103231",
"proprietary_names": [
"Kyphon Inflation Syringe"
]
},
{
"product_code": "NEK",
"device_name": "Filler, Recombinant Human Bone Morphogenetic Protein, Collagen Scaffold With Metal Prosthesis, Osteoinduction",
"device_class": "3",
"medical_specialty": "Unknown",
"regulation_number": null,
"clearance": "P000058",
"proprietary_names": [
"INFUSE BONEGRAFT/ LT-CAGE Lumbar TF"
]
},
{
"product_code": "NQO",
"device_name": "Prosthesis, Spinous Process Spacer/Plate",
"device_class": "3",
"medical_specialty": "Unknown",
"regulation_number": null,
"clearance": "P040001",
"proprietary_names": [
"X-STOP® Interspinous Spacer Titanium"
]
}
]
}
]
},
"evidence": {
"source": "US Food and Drug Administration",
"source_kind": "public",
"retrieved_at": "2026-10-21T00:00:00.000Z",
"calls": [
{
"retrieved_at": "2026-10-21T00:00:00.000Z"
}
],
"as_of": "2026-10-12"
}
}
}
See Pricing for this tool’s price. A wallet (x402) call receives it in the 402 quote before anything is charged; a call paid from prepaid credits is charged when the API accepts the request and answers
200.Notes
- Results return inline. The finished job stays available at
/v1/requests/{request_id}