FDA Device Intelligence
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Retractor, Fiberoptic

FDA product code FDG · Class 1 · Gastroenterology, Urology

402
Registered devices
89
Adverse events
2
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2009-07-01Lumitex IncAdhesive which is used to attach LightMat to retractor may not have been tested to Medical standards. The vendor provided an adhesive strip that did not confor
2008-10-24Biomet Microfixation, Inc.Fiber optic cable is missing from the Frederick's Converse Retractor Lot # 042408D08.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.