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Synergetics
SYNERGETICS USA, INC. · Model 56.20.23P · UDI-DI 20841305107261
MPA
Prescription
10
510(k) clearances
270
Adverse events
1
Recalls
30
Facilities
Description
23ga Vivid™ Endo Illuminator
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-08-05 | Alcon Research LLC | Due to incomplete seals in the pouch which provide 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.