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X402stock · FDA

by X402stock

GETBase

$0.03

per call · USD Coin on Base

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).

Endpoint

GET https://x402stock.xyz/api/v1/fda

1

Calls / 30d

1

Unique payers / 30d

Aug 17

Last called

exact

Payment scheme

Call this service

TypeScript · @x402/fetch
import { wrapFetchWithPayment } from "@x402/fetch";
import { privateKeyToAccount } from "viem/accounts";

const account = privateKeyToAccount(process.env.PRIVATE_KEY);
const fetchWithPay = wrapFetchWithPayment(fetch, account);

const res = await fetchWithPay("https://x402stock.xyz/api/v1/fda", {
  method: "GET",
});
const data = await res.json();
cURL
curl -X GET \
  "https://x402stock.xyz/api/v1/fda?company=Pfizer&limit=10" \
  -H "X-PAYMENT: <signed x402 payment>"

Example response

{
  "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"
}

Payment details

Pay to0x3070fbb3803819fb5bdfe9286fdc6325a877fa85
AssetUSD Coin · 0x833589fcd6edb6e08f4c7c32d4f71b54bda02913
NetworksBase
Schemesexact

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