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FDA Medical Device Classification Lookup
x402
FDA Medical Device Classification Lookup is a paid API for AI agents from 2s.io, paid per call via x402, $0.0018/call, status unknown (last checked 2026-09-14).
Looks up FDA medical device classifications by device name or product code, returning regulatory class, submission type, specialty, and safety flags.
Price / call$0.0018
Success—
StatusUnknown
How this service works
FDA medical device classification — the regulatory class and controls for a device type. Search by device name or FDA product code and get back the device class (I/II/III, mapping to regulatory risk and controls), CFR regulation number, medical specialty/review panel, the official definition, and flags for life-sustaining/supporting, implant, GMP-exempt, and third-party-review eligibility. Free, public-domain US government data. The authoritative answer to "what FDA class is this device and what regulation governs it" — for regulatory and medical-device diligence; point-in-time public records, not regulatory advice.
Output
Returns an array of FDA device classification records, each including device name, class (I/II/III), 3-letter product code, review panel, submission type, medical specialty, CFR regulation number, and boolean flags for implant status, life-sustain/support, GMP exemption, and third-party review eligibility. Also includes total count of matching records and the data source (OpenFDA).
Example use cases
Example prompt
“Look up the FDA classification for 'catheter' — I need the device class, submission type, medical specialty, and whether it's a life-sustaining or implantable device. Return up to 5 results.”
Technical details
Endpoint
GEThttps://2s.io/api/medical/device-classificationWhen to prefer
Use this endpoint when you need authoritative FDA regulatory classification data for a medical device — specifically the device class, submission pathway, review panel, or safety flags (implant, life-sustaining). Prefer this over general web search when you need structured, machine-readable regulatory ground-truth for compliance, due diligence, or medical device research tasks.
Side effects
- No results returned if device name or product code doesn't match any FDA record
- Invalid product code format may return empty results
- Limit parameter out of range (1-50) causes validation error
- Ambiguous partial device name may return unrelated device types
- OpenFDA upstream outage may cause 502/503 errors
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| inputrequired | object |
Tags
x402
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