FDA Device Intelligence
Home › AMERICAN DIAGNOSTIC CORP › ADC®

ADC®

AMERICAN DIAGNOSTIC CORP · Model 39708 · UDI-DI 00634782098285

KQW
10
510(k) clearances
4
Adverse events
0
Recalls
81
Facilities

Description

8" Goniometer 360 Degree,

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.