Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003934980

FEI Number

3003934980

Entity Name

VECTOR RESEARCH & DEVELOPMENT

City/State/Country

UNIVERSITY PLACE, WA, US

Establishment Address

2810 69th Ave West, UNIVERSITY PLACE, WA 98466, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

VECTOR RESEARCH & DEVELOPMENT (Owner Number: 9049244)

Owner / Operator Contact Address

2810 69th Ave West, --, University Place, WA 98466, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K023545

PMA Number

N/A

All Registered Proprietary Names

Vector Vector Vector Vector Quazar Q-Light Vector Vector Vector Enbio Vector Vector

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EFB	Handpiece, Air-Powered, Dental	Dental	Class 1	872.4200	2021-04-02
EFB	Handpiece, Air-Powered, Dental	Dental	Class 1	872.4200	2017-12-19
ELC	Scaler, Ultrasonic	Dental	Class 2	872.4850	2016-03-25
EBW	Controller, Foot, Handpiece And Cord	Dental	Class 1	872.4200	2016-03-25
EBZ	Activator, Ultraviolet, For Polymerization	Dental	Class 2	872.6070	2021-04-02
EFB	Handpiece, Air-Powered, Dental	Dental	Class 1	872.4200	2020-03-09
EFB	Handpiece, Air-Powered, Dental	Dental	Class 1	872.4200	2016-03-25
EBZ	Activator, Ultraviolet, For Polymerization	Dental	Class 2	872.6070	2016-03-25
FLE	Sterilizer, Steam	General Hospital	Class 2	880.6880	2022-06-15
ELC	Scaler, Ultrasonic	Dental	Class 2	872.4850	2016-03-25
EBZ	Activator, Ultraviolet, For Polymerization	Dental	Class 2	872.6070	2017-12-19

Official Correspondent

BRENT BIGLER

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VECTOR RESEARCH & DEVELOPMENT

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
K212910	Shenzhen Carejoy Technology Co., Ltd.	Dental High-speed Turbine Handpiece, Dental Low-speed Turbine Handpiece	2022-11-17
K832443	California Technics, Inc.	ULTRASONIC DENTAL PROPHYLAXIS UNIT	1983-09-12
K994299	Bonart Co., Ltd.	ART-P3, MODEL P3-1-ART-A1	2000-03-06
K040153	Indigenous Peoples Technology and Education Center	I-TEC PORTABLE DENTAL OPERATORY	2004-05-21
K243921	Foshan Coxo Medical Instrument Co., Ltd.	LED Curing Lights (DB686 HALO)	2025-04-11

Similar Registrations

Registration Number	Establishment Name	Location
3017619674	FOSHAN WENJIAN MEDICAL INSTRUMENT CO., LTD.	Foshan Guangdong, CN
3014471275	TUNAP GMBH & CO. KG	Wolfratshausen Bavaria, DE
2133714	INTER-MED, INC.	Racine, WI, US
2246821	MTI PRECISION PRODUCTS	Coatesville, PA, US
8010468	GEBR. BRASSELER GMBH & CO. KG	LEMGO North Rhine-Westphalia, DE

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003934980. Last updated year: 2026. Please use registration number 3003934980 when referencing this establishment in official correspondence.