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OPTOMIC ESPAÑA SA · Model Fibrolux LED HP Light Source (Amber) · UDI-DI 08436041580140
10
510(k) clearances
36
Adverse events
1
Recalls
99
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2007-02-07 | Boston Scientific Corporation | Light Degradation in transmission-A film may deposit on the front face and limit transmission of light |
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Get your free API keyRead the docsData 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.