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Burr, Corneal, Battery Powered, Rust Ring Removal

FDA product code OHW · Class 1 · Ophthalmic

57
Registered devices
0
Adverse events
1
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2016-10-12Bausch & Lomb, Inc.According to firm ( Bausch & Lomb, Inc. ) on June 17, 2016 a packaging operator notified his supervisor he had not placed the operating instruction into the la

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