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Evacuator, Vapor, Cement Monomer

FDA product code JDY · Class 1 · Orthopedic

16
Registered devices
19
Adverse events
1
Recalls
8
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2008-06-30Zimmer Inc.The cartridge is brittle and at increased risk of breakage.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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