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Laparoscopic Bone Anchor Urethropexy Instrument Kit

FDA product code NWN · Class 2 · Orthopedic

5
Registered devices
1
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2025-11-11Medline Industries, LPThere have been multiple complaints of drill bit fusing to the bushing/sleeve within the drill guide during use. Retrieving a replacement drill bit and drill gu

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