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Saylor Innovations FDA Device Classification
x402
Saylor Innovations FDA Device Classification is a paid API for AI agents from saylorinnovations.com, paid per call via x402, $0.01/call, status unknown (last checked 2026-10-30).
Looks up FDA medical device classification by device name, returning class (I–III), product code, regulation number, medical specialty, and implant/life-sustaining flags
Price / call$0.01
Success—
StatusUnknown
How this service works
FDA medical device classification by name - device class I to III, product code, regulation number, specialty, implant and life-sustaining flags
Output
Returns a JSON object with the interpreted query string, total match count, and an array of matching device records. Each record includes the device name, device class (I, II, or III), product code, regulation number, medical specialty, review panel, submission type, GMP exemption status, a human-readable definition, and boolean flags for implant and life-sustaining status.
Example use cases
Regulatory check for a new medical device
“We're launching a portable ECG monitor — can you look up its FDA device classification, product code, and whether it's considered life-sustaining or an implant?”
Compliance screening for hospital procurement
“Before we purchase these bone screws for the OR, can you check the FDA classification to confirm whether they're Class II or III and if they're flagged as implants?”
Medical device startup due diligence
“I'm evaluating a startup that makes insulin pumps — can you pull the FDA classification, regulation number, and submission type for insulin pumps so I understand the regulatory burden?”
Technical details
Endpoint
GEThttps://saylorinnovations.com/api/devices/classification?utm_source=zero.xyzWhen to prefer
Use this endpoint when you need fast, structured FDA classification data for a medical device by name, especially when you need class, product code, regulation number, and implant/life-sustaining flags in a single call. Prefer this over manually querying the FDA 510(k) database or parsing FDA product code tables. Ideal for regulatory compliance checks, procurement screening, or device due diligence workflows where a quick per-device lookup at low cost ($0.01/call) is acceptable.
Side effects
- No matching devices found for an obscure or misspelled device name — returns empty devices array
- Ambiguous query returns many unrelated devices — caller should refine query or inspect total_matches
- Limit parameter out of range (must be 1–25) may be ignored or cause an error
- Service unavailable or upstream FDA data unreachable — HTTP 5xx response
- Missing required 'q' query parameter returns a 400-level error
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object | |
| output | object |
Tags
x402
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