FDA Device Intelligence
Home › OPTOMIC ESPAÑA SA › Optomic

Optomic

OPTOMIC ESPAÑA SA · Model OP-C5 COLPOSCOPE · UDI-DI 08436041580102

PTZ
0
510(k) clearances
2
Adverse events
0
Recalls
15
Facilities

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.