api.govparse.io · /v1/feeds/fda-device-clearances
Which medical devices did the FDA just clear or approve, and who is the applicant? Bulk feed over openFDA 510(k) clearances and PMA approvals, newest-first by decision date — a new clearance is a device launch. Cursor-paginated up to 1000/page, filterable by applicant, state, product code, pathway (510k/pma), advisory committee, or since. Rows carry the applicant, device name, product code, advisory committee, pathway, and decision. Observational public records, never a recommendation.
Listing completeness · 80/100
Presence of published information only. Not a security, reliability or performance score. Same rules for Datoka and external listings.
- Name and traceable source
- 10/10 · Present
- Meaningful description
- 10/10 · Present
- Connection or installation reference
- 20/20 · Present
- Dedicated documentation or source repository
- 0/15 · Missing or insufficient
- Explicit free access or numeric tariff
- 20/20 · Present
- Declared integration protocol
- 10/10 · Present
- Source updated within 90 days
- 10/10 · Present
- Declared capability names
- 0/5 · Missing or insufficient
Evaluated 2026-10-08 · Method listing-completeness-1. Scoring rules
Connect & use
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x402 resource
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Categories and declared capabilities
Topic categories are derived from publisher text for discovery, not independently verified capabilities.
The registry does not provide a verified tools list. See the observations, when available, for any tools/list check; a published tools list does not establish that execution succeeds.
Evidence, with its limits.
This listing is indexed. Any domain claim or endpoint observation appears separately with its date and limited scope. No payment execution, factual accuracy or safety certification is inferred.