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x402stock FDA Data API
x402
x402stock FDA Data API is a paid API for AI agents from x402stock.xyz, paid per call via x402, $0.03/call, status unknown (last checked 2026-10-20).
Returns FDA drug recalls, drug approvals, device approvals, and device clearances for a named company, paid per-call in USDC via x402
Price / call$0.03
Success—
StatusUnknown
How this service works
FDA catalysts for a pharma/biotech/medtech company, from openFDA. Pass `?company=Medtronic` (required) plus `?limit=` (max 50). Returns `drug` (recalls + approvals) and `device` (510(k) clearances, PMA approvals, recalls) sections, each with recent items, match totals, and official FDA links. One call across 5 FDA datasets. From x402stock, a market & economic data API (x402, USDC).
Output
A JSON object containing the company name, timestamp, and four data buckets: drug recalls (with date, status, classification, product description, recall reason, firm, recall number, voluntary/mandated flag), drug approvals, device PMA approvals (with applicant, PMA number, trade name, generic name, decision date, supplement type, advisory committee), and device 510k clearances (with K-number, applicant, device name, decision, dates, advisory committee). Each bucket reports count and total_matched.
Example use cases
Example prompt
“Pull the FDA drug recalls, drug approvals, device approvals, and device clearances for Medtronic — show me up to 10 results per category.”
Technical details
Endpoint
GEThttps://x402stock.xyz/api/v1/fda?utm_source=zero.xyzWhen to prefer
Use this endpoint when an AI agent needs structured, aggregated FDA regulatory data — recalls, approvals, and clearances — for a specific company without managing API keys or subscriptions. It is ideal for financial analysis of pharma/medtech stocks, due diligence workflows, compliance checks, or news enrichment. Prefer over direct openFDA queries when you want company-centric aggregation across multiple FDA databases in one call, and pay only per request.
Side effects
- Unknown or misspelled company name returns empty result sets with total_matched 0
- limit parameter out of range (<=0 or >50) causes validation error
- Company name too short (<2 chars) or too long (>120 chars) causes input validation failure
- FDA upstream (openFDA) unavailable causes 5xx or timeout
- Payment not confirmed via x402 returns 402 Payment Required
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Output
Schema · Response
{
"type": "json",
"example": {
"drug": {
"recalls": {
"count": 0,
"items": [],
"total_matched": 0
},
"approvals": {
"count": 0,
"items": [],
"total_matched": 0
}
},
"as_of": "2026-06-18T12:00:00.000Z",
"device": {
"recalls": {
"count": 0,
"items": [],
"total_matched": 1250
},
"approvals": {
"count": 1,
"items": [
{
"url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P160043",
"applicant": "Medtronic Vascular",
"pma_number": "P160043",
"trade_name": "Resolute Onyx Zotarolimus-Eluting Coronary Stent System",
"generic_name": "Coronary drug-eluting stent",
"product_code": "NIQ",
"decision_code": "OK30",
"decision_date": "2026-06-05",
"supplement_type": "30-Day Notice",
"supplement_number": "S094",
"advisory_committee": "Cardiovascular"
}
],
"total_matched": 12772
},
"clearances": {
"count": 1,
"items": [
{
"url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K253656",
"decision": "Substantially Equivalent",
"k_number": "K253656",
"applicant": "Medtronic Sofamor Danek USA, Inc.",
"device_name": "OsteoCool RF Ablation System; OsteoCool 2.0 RF Ablation System",
"product_code": "GEI",
"date_received": "2025-11-20",
"decision_date": "2026-06-05",
"clearance_type": "Traditional",
"advisory_committee": "General, Plastic Surgery"
}
],
"total_matched": 1576
}
},
"source": "fda",
"company": "Medtronic",
"attribution": "Source: openFDA, U.S. Food and Drug Administration"
}
}Tags
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