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Sklar
SKLAR CORPORATION · Model 55-7087 · UDI-DI 10649111012471
5
510(k) clearances
10
Adverse events
1
Recalls
206
Facilities
Description
MICRO DISS & VASC SPATULA 8.5 INCHES
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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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.