W&H DENTALWERK BUERMOOS GMBH
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
Devices registered here (1)
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentProduct code HWE (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4820
Recalls & enforcement
- Class IIOngoing2024-01-161:2 speed increasing surgical handpieces have been incorrectly laser marked during production. The specific laser marking should read 1:2, but instead it reads 1:1 on the body of the handpiece
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “W&H DENTALWERK BUERMOOS GMBH (FEI 3003755849) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3003755849-w-h-dentalwerk-buermoos-gmbh/
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