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K 180 OPHTHALMOSCOPE

Heine Optotechnik GmbH & Co. KG · Model 2,5 V · UDI-DI 04053755120017

HLJ
10
510(k) clearances
5
Adverse events
0
Recalls
63
Facilities

Description

since 2024-05 in LED version: K180 LED ophthalmoscope

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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.