# toolcall.click Medical Device Intelligence

> toolcall.click Medical Device Intelligence is a paid API for AI agents from toolcall.click, paid per call via x402, $0.04/call, status down (last checked 2026-09-15).

Aggregates FDA intelligence on any medical device — GUDID identity, device class, 510(k)/PMA status, recalls, and MAUDE adverse-event counts — from openFDA in a single call

## Facts

- Endpoint: GET https://toolcall.click/t/med/device
- Price: $0.04/call
- Payment: x402
- Status: down
- Last checked: 2026-09-15
- Activations on Zero: 0
- Tags: x402
- Canonical page: https://www.zero.xyz/c/toolcall-click-medical-device-intelligence-743915e7
- Structured record (JSON): https://api.zero.xyz/v1/capabilities/cap_xIVUmYghfYIfUgV_jBf8B

Status and success rate cover calls made through Zero and Zero's own probes. Third-party monitors may report differently.

## How to call it through Zero

Zero handles the 402 payment challenge and records the run. With the Zero CLI installed (`npm i -g @zeroxyz/cli`):

```sh
zero fetch --capability toolcall-click-medical-device-intelligence-743915e7
```

Example prompt: Pull up the full FDA regulatory profile for the Abbott FreeStyle Libre — I need the device class, whether it has 510(k) clearance or PMA approval, any recent recalls, and how many adverse events are on file in MAUDE.

## When to prefer this

Use this endpoint when you need a single-call FDA regulatory summary for a medical device, combining identity, classification, clearance/approval history, recall status, and adverse events from openFDA without having to query multiple FDA databases separately. Prefer over direct openFDA queries when you want aggregated intelligence in one response. Best for regulatory due diligence, device safety checks, competitive research, or compliance workflows.

## Known failure modes

- Device not found in openFDA — returns empty or null results if name/UDI doesn't match any record
- Ambiguous device name matches multiple products — may return data for wrong device; use UDI for precision
- openFDA API upstream outage — may return 502/503 or timeout
- Invalid UDI format — returns error if DI is malformed
- Rate limiting or payment failure — call not processed if x402 payment is rejected

## How this service works

Keyless pay-per-call APIs for AI agents: 30 tools across compliance, trade, safety, web and data. Pay per call with USDC on Base via x402. No account, no API key.

## Output

A JSON object containing aggregated FDA data for the queried device: GUDID identity fields (product name, manufacturer, UDI), device classification and regulation number, list of 510(k) clearances and/or PMA approvals, recent recall records, and a count of MAUDE adverse-event reports — all sourced live from openFDA in one response.

## Response schema (JSON Schema)

```json
{
 "type": "json",
 "example": {
  "recalls": [],
  "classification": [
   {
    "class": "2",
    "deviceName": "Pump, Infusion, Insulin",
    "regulation": "880.5725"
   }
  ],
  "clearances510k": [
   {
    "kNumber": "K123456",
    "applicant": "Example Medical",
    "decisionDate": "2024-05-01"
   }
  ],
  "adverseEventReports": 51234
 }
}
```

## More

- Live health (JSON, refreshed every minute): https://www.zero.xyz/c/toolcall-click-medical-device-intelligence-743915e7/health.json
- [Zero catalog index](https://www.zero.xyz/llms.txt)
- [Other services from toolcall.click](https://www.zero.xyz/host/toolcall.click/llms.txt)