Medical Device Manufacturer · US , Placentia , CA

Handpiece Headquarters - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2009

Total

Cleared

Denied

Handpiece Headquarters has 6 FDA 510(k) cleared medical devices. Based in Placentia, US.

Latest FDA clearance: Dec 2024. Active since 2009. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Handpiece Headquarters Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.

FDA 510(k) Regulatory Record - Handpiece Headquarters

6 devices

1-6 of 6

Data Source

Sourced from the FDA 510(k) public files . 174,883 total devices indexed.

Last updated: May 10, 2026