Handpiece Headquarters - HPR Inc.
1 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (1)
Devices registered here (1)
- Handpiece, Air-Powered, DentalProduct code EFB (opens in a new tab) · Class I · Dental · 21 CFR 872.4200
Recalls & enforcement
- Class IIOngoing2018-04-04Tip of the curing light was too hot causing a heat sensation in the patients.
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. “Handpiece Headquarters - HPR Inc. (FEI 3007007357) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007007357-handpiece-headquarters-hpr-inc/
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