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Saw, Manual And Accessories

FDA product code GDR · Class 1 · General, Plastic Surgery

241
Registered devices
5
Adverse events
1
Recalls
2
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2017-05-11Argon Medical Devices, IncArgon Medical has received a complaint from one of their distributors of a potential packaging defect. The product is sealed in a pouch and the defect if prese

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