FDA applicant
Handpiece Headquarters, Inc. - Hpr, Inc.
FDA records 3 decisions for Handpiece Headquarters, Inc. - Hpr, Inc. (Placentia, CA) from 2008 to 2019: 3 510(k) clearances. Most are in product codes EFB (Handpiece, Air-Powered, Dental) and EBW (Controller, Foot, Handpiece And Cord). Its devices cite 3 predicates, 0 of them its own earlier devices. No recall is linked to its devices.
FDA’s records also spell it “Handpiece Headquarters - Hpr, Inc.”.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Handpiece Headquarters, Inc. - Hpr, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
1in 2019
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2008.
Planning a device like Handpiece Headquarters, Inc. - Hpr, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Handpiece”
FDA records each applicant name separately; these may or may not be the same firm.