FDA Device Intelligence
Home › FMD, LLC › DUROSCOPE

DUROSCOPE

FMD, LLC · Model UHD-631 · UDI-DI 00863333000334

FWL
2
510(k) clearances
3
Adverse events
0
Recalls
33
Facilities

Description

UHD Camera

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.