FDA Device Intelligence
HomeAMERICAN DIAGNOSTIC CORP › Diagnostix.

Diagnostix.

AMERICAN DIAGNOSTIC CORP · Model 5680A-349W · UDI-DI 00634782090401

HLJERAFLL
2
510(k) clearances
5
Adverse events
0
Recalls
63
Facilities

Description

Adstation Oto+-L/Coax Oph-X,429, 9005W/Spec Disp, WB

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.