Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007007357

FEI Number

3007007357

Entity Name

Handpiece Headquarters

City/State/Country

Placentia, CA, US

Establishment Address

620 S. Placentia Ave., Placentia, CA 92870, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Handpiece Headquarters (Owner Number: 10028763)

Owner / Operator Contact Address

620 S. Placentia Ave., Placentia, CA 92870, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K180845

PMA Number

N/A

All Registered Proprietary Names

BASE290 LED Curing Light Maxima Advanced 3000 LED Curing Light QualityPlus DHR Score HHC Medidenta Air King Prophy Magic HPR Cordless Hygiene Handpiece Carina GEM Latch Contra Angle 20K Deluxe Sectional Ball Bearing Latch Contra Angle 40K Friction Grip Contra Angle 20K Deluxe Sectional Latch Contra Angle 20K Deluxe Sectional Friction Grip Contra Angle 20K Ball Bearing Latch Contra Angle 40K ChoicePro Thor 700+ Medilectric

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EBZ	Activator, Ultraviolet, For Polymerization	Dental	Class 2	872.6070	2023-11-09
EFB	Handpiece, Air-Powered, Dental	Dental	Class 1	872.4200	2009-03-04
EKX	Handpiece, Direct Drive, Ac-Powered	Dental	Class 1	872.4200	2024-12-23
MUH	System, X-Ray, Extraoral Source, Digital	Dental	Class 2	872.1800	2024-08-21
EGS	Handpiece, Contra- And Right-Angle Attachment, Dental	Dental	Class 1	872.4200	2016-02-25
EBW	Controller, Foot, Handpiece And Cord	Dental	Class 1	872.4200	2019-09-06

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Handpiece Headquarters

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K243921	Foshan Coxo Medical Instrument Co., Ltd.	LED Curing Lights (DB686 HALO)	2025-04-11
K033201	Apoza Enterprise Co., Ltd.	LA500 BLUE LIGHT	2003-12-02
K212910	Shenzhen Carejoy Technology Co., Ltd.	Dental High-speed Turbine Handpiece, Dental Low-speed Turbine Handpiece	2022-11-17
K241065	Dentis Co., Ltd.	ChecQ (AC100)	2025-03-21
K221008	Shanghai Handy Medical Equipment Co., Ltd.	HDR Sensor- HDR361 (Size 1), HDR Sensor- HDR461 (Size 2)	2022-06-22

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3030126955	ONVET MEDICAL CANADA INC	TORONTO Ontario, CA
1419489	NORDENT MFG., INC.	ELK GROVE VILLAGE, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007007357. Last updated year: 2026. Please use registration number 3007007357 when referencing this establishment in official correspondence.