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mirrored listing x402 eip155:8453solana:5eykt4UsFv8P8NJdTREpY1vzqKqZKvdp

Which companies just cleared or got FDA approval for a medical device? Search openFDA devi

Which companies just cleared or got FDA approval for a medical device? Search openFDA device 510(k) clearances and PMA premarket approvals by applicant company, pathway (510k/pma), FDA product code, advisory-committee specialty (e.g. Cardiovascular), applicant state, or decision date (since). Returns the applicant company (entity-resolved where possible), device name, product code, and decision date — a fresh target list for device and component sellers. openFDA public-domain records.

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1250000 (raw units)
price
1
calls / 30d
1
unique payers
2026-09-08
updated

Provider

api.govparse.io · discovered, not yet claimed by its owner

Payment (x402 accepts[])

[
  {
    "scheme": "exact",
    "network": "eip155:8453",
    "payTo": "0x3873d15CF3209c32aaA8d9AA542164E658567129",
    "asset": "0x833589fCD6eDb6E08f4c7C32D4f71b54bdA02913",
    "amount": "1250000",
    "maxTimeoutSeconds": 300
  },
  {
    "scheme": "exact",
    "network": "solana:5eykt4UsFv8P8NJdTREpY1vzqKqZKvdp",
    "payTo": "BdcZbENFdEyEUMqv9pnRMUnn1Yyeyo2dCMbYXbJ3LmaB",
    "asset": "EPjFWdd5AufqSSqeM2qN1xzybapC8G4wEGGkZwyTDt1v",
    "amount": "1250000",
    "maxTimeoutSeconds": 300
  }
]

Output schema

{
  "bazaar": {
    "info": {
      "input": {
        "method": "GET",
        "queryParams": {
          "company": "Medtronic",
          "pathway": "510k",
          "product_code": "DXY"
        },
        "type": "http"
      },
      "output": {
        "example": {
          "rows": [
            {
              "advisory_committee": "Cardiovascular",
              "applicant": "Pacesetter Systems",
              "clearance_type": "Traditional",
              "date_received": "1985-02-19",
              "decision_code": "SESE",
              "decision_date": "1985-04-01",
              "decision_description": "Substantially Equivalent",
              "decision_id": "K850651",
              "device_name": "PROGRAMALITH III-3 MODEL 231 PULSE GENERATOR",
              "entity_id": null,
              "generic_name": null,
              "pathway": "510k",
              "product_code": "DXY",
              "state": "CA"
            }
          ],
          "total_matched": 1
        },
        "type": "json"
      }
    },
    "routeTemplate": "/v1/fda/device-clearances/search",
    "schema": {
      "$schema": "https://json-schema.org/draft/2020-12/schema",
      "properties": {
        "input": {
          "properties": {
            "advisory_committee": {
              "description": "Medical specialty panel fragment.",
              "examples": [
                "Cardiovascular"
              ],
              "type": "string"
            },
            "company": {
              "description": "Applicant company — suffix/punctuation-insensitive.",
              "examples": [
                "Medtronic"
              ],
              "type": "string"
            },
            "entity_id": {
              "description": "Resolved employer entity UUID.",
              "examples": [
                "b7f3e2d1-4a5c-4e6f-8a9b-0c1d2e3f4a5b"
              ],
              "type": "string"
            },
            "limit": {
              "description": "Max rows (default 25, cap 100).",
              "examples": [
                25
              ],
              "type": "integer"
            },
            "offset": {
              "description": "Rows to skip.",
              "examples": [
                0
              ],
              "type": "integer"
            },
            "pathway": {
              "description": "510k | pma (CSV).",
              "examples": [
                "510k"
              ],
              "type": "string"
            },
            "product_code": {
              "description": "FDA product code(s), CSV.",
              "examples": [
                "DXY"
              ],
              "type": "string"
            },
            "since": {
              "description": "Decision (clearance/approval) date on/after this date (YYYY-MM-DD).",
              "examples": [
                "2026-01-01"
              ],
              "type": "string"
            },
            "sort": {
              "description": "decision_date | date_received :asc|:desc. Default decision_date:desc.",
              "examples": [
                "decision_date:desc"
              ],
              "type": "string"
            },
            "state": {
              "description": "Applicant state code(s), CSV (510(k) only).",
              "examples": [
                "CA"
              ],
              "type": "string"
            }
          },
          "required": [],
          "type": "object"
        }
      },
      "type": "object"
    }
  }
}

Use it

curl

curl "https://api.govparse.io/v1/fda/device-clearances/search"
# -> 402 Payment Required, accepts[] lists how to pay
# retry with a PAYMENT-SIGNATURE (or PAYMENT header) once paid

JavaScript

const res = await fetch("https://api.govparse.io/v1/fda/device-clearances/search");
if (res.status === 402) {
  const { accepts } = await res.json();
  // pay one of accepts[] via an x402 client, then retry with the payment header
}

Python

import httpx
res = httpx.get("https://api.govparse.io/v1/fda/device-clearances/search")
if res.status_code == 402:
    accepts = res.json()["accepts"]
    # pay one of accepts[] via an x402 client, then retry with the payment header

Machine-readable

Everything on this page is also available as clean JSON at /resources/14578.json, and this resource appears in /discovery/resources and /discovery/search.