Request
{
"method": "GET",
"queryParams": {
"company": "Pfizer",
"limit": 10
},
"type": "http"
}
Response
{
"example": {
"as_of": "2026-06-18T12:00:00.000Z",
"attribution": "Source: openFDA, U.S. Food and Drug Administration",
"company": "Medtronic",
"device": {
"approvals": {
"count": 1,
"items": [
{
"advisory_committee": "Cardiovascular",
"applicant": "Medtronic Vascular",
"decision_code": "OK30",
"decision_date": "2026-06-05",
"generic_name": "Coronary drug-eluting stent",
"pma_number": "P160043",
"product_code": "NIQ",
"supplement_number": "S094",
"supplement_type": "30-Day Notice",
"trade_name": "Resolute Onyx Zotarolimus-Eluting Coronary Stent System",
"url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P160043"
}
],
"total_matched": 12772
},
"clearances": {
"count": 1,
"items": [
{
"advisory_committee": "General, Plastic Surgery",
"applicant": "Medtronic Sofamor Danek USA, Inc.",
"clearance_type": "Traditional",
"date_received": "2025-11-20",
"decision": "Substantially Equivalent",
"decision_date": "2026-06-05",
"device_name": "OsteoCool RF Ablation System; OsteoCool 2.0 RF Ablation System",
"k_number": "K253656",
"product_code": "GEI",
"url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253656"
}
],
"total_matched": 1576
},
"recalls": {
"count": 0,
"items": [],
"total_matched": 1250
}
},
"drug": {
"approvals": {
"count": 0,
"items": [],
"total_matched": 0
},
"recalls": {
"count": 0,
"items": [],
"total_matched": 0
}
},
"source": "fda"
},
"type": "json"
}