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Punch, Biopsy, Surgical

FDA product code EME · Class 1 · Dental

250
Registered devices
6
Adverse events
1
Recalls
3
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2021-03-30Omnia SRLOmnia SRL received a notification from the contract manufacturer informing them of inadequate sterilization processes which have been taking place at their cont

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