FDA Device API

Provides access to FDA data on medical devices marketed in the United States, including adverse event reports, product classifications, 510(k) clearances, and premarket approvals. Also covers device recalls, unique device identifiers, establishment registrations, and COVID-19 serology test performance data.

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Screenshot:
Screenshot of FDA Device API homepage
Slug: fda-device
Key: fda.gov:fda-device-api
Base URL: https://api.fda.gov/device/
Auth: none
Endpoints: 15
Reachable: yes
CORS: unknown
Tier: verified
Last checked: 2026-03-14 22:14:49.893526

Links

Homepage: https://open.fda.gov/
API Base: https://api.fda.gov/device/
Documentation:

Topics

HEALTH

Tutorials

Skills

Endpoints (15)

Path Summary Response Auth
510k.json Search 510(k) premarket notifications application/json
classification.json Search device classifications application/json
device/510k.json Search 510(k) premarket notifications application/json
device/classification.json Search device classifications application/json
device/covid19serology.json COVID-19 Serological Testing application/json
device/enforcement.json Device Enforcement Reports application/json
device/event.json Search medical device adverse events application/json
device/pma.json Search PMA premarket approvals application/json
device/recall.json Search device recalls application/json
device/registrationlisting.json Device Registration and Listing application/json
device/udi.json Search Unique Device Identification database application/json
event.json Search device adverse event reports application/json
pma.json Search PMA premarket approvals application/json
recall.json Search device recalls application/json
registrationlisting.json Search device registration and listing application/json