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Diagnostix™

AMERICAN DIAGNOSTIC CORP · Model 56802X-35EU · UDI-DI 00634782089986

HLJ ERA IBJ

510(k) clearances

Adverse events

Recalls

Facilities

Description

Adstation Oto+-X/Coax+Oph-X,Derm/Spec Disp, EU

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

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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.