FDA applicant

Handpiece Headquarters

Placentia, CA6 decisions2009–20240 recalls

FDA records 6 decisions for Handpiece Headquarters (Placentia, CA) from 2009 to 2024: 6 510(k) clearances. Most are in product codes EGS (Handpiece, Contra- And Right-Angle Attachment…) and EFB (Handpiece, Air-Powered, Dental). Its devices cite 5 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Handpiece Headquarters’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2009high 1 (2009) · low 0 (2011)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2009.

FIG. 1 — Handpiece Headquarters by year, 2009–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Handpiece Headquarters’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) Report

Other applicant names beginning “Handpiece”

FDA records each applicant name separately; these may or may not be the same firm.

Handpiece Headquarters, Inc. - Hpr, Inc. 3 Handpiece Club, LLC 1 Handpiece Unlimited 1

Handpiece Headquarters

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Handpiece”