Handpiece Headquarters
Handpiece Headquarters holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2024, with 1 FDA device recall on record.
Top product codes for Handpiece Headquarters
FDA recalls by Handpiece Headquarters
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Handpiece Headquarters
- K243911 — HPR Cordless Hygiene Handpiece
- K233518 — BASE290 LED Curing Light
- K143183 — Maxima XTEND Handpiece Maintenance System
- K141125 — U-TYPE CONTRA ANGLE, U-TYPE SECTIONAL CONTRA ANGLE
- K100389 — HHC PUSH-BUTTON REPLACEMENT TURBINE FOR MIDWEST TRADITION HANDPIECE MODEL MW TURBINE REPLACEMENT
- K092053 — MAXIMA-M STRAIGHT ATTACHMENT, MAXIMA-M CONTRA ANGLE SHEATH
Data sourced from openFDA. This site is unofficial and independent of the FDA.