Data / Medical devices / United States / Vector Research & Development
Vector Research & Development: FDA-registered device maker in University Place, WA, United States, 18 510(k) clearances
Vector Research & Development is registered with the FDA (registration 3003934980) in University Place, WA, United States. It lists 7 device types. The FDA files 18 510(k) clearances under its listings, the newest dated February 22, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3003934980
- Address
- 2810 69th Ave West, University Place, WA, United States, 98466
- Owner or operator
- VECTOR RESEARCH & DEVELOPMENT (9049244)
- Roles
- Repackager or relabeler
- First device listed
- March 25, 2016
- Registered through
- 2026
- Brand names listed
- Enbio, MaxRay, MaxRay W68, Quazar Q-Light, Vector
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Activator, Ultraviolet, For Polymerization | EBZ | 2 | Repackager or relabeler | accessdata.fda.gov |
| Controller, Foot, Handpiece And Cord | EBW | 1 | Repackager or relabeler | accessdata.fda.gov |
| Handpiece, Air-Powered, Dental | EFB | 1 | Repackager or relabeler | accessdata.fda.gov |
| Scaler, Ultrasonic | ELC | 2 | Repackager or relabeler | accessdata.fda.gov |
| Sterilizer, Steam | FLE | 2 | Repackager or relabeler | accessdata.fda.gov |
| System, X-Ray, Extraoral Source, Digital | MUH | 2 | Repackager or relabeler | accessdata.fda.gov |
| Unit, X-Ray, Extraoral With Timer | EHD | 2 | Repackager or relabeler | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 22, 2022 | K213991 | Enbio S | FLE | Substantially Equivalent | Enbio Group AG | accessdata.fda.gov |
| October 26, 2017 | K173046 | Cocoon Portable Handheld X-Ray System | MUH | Substantially Equivalent | Dexcowin Co., Ltd. | accessdata.fda.gov |
| December 8, 2015 | K152146 | High Speed Handpieces and Accessories | EFB | Substantially Equivalent | Codent Technical Industry Co., Ltd. | accessdata.fda.gov |
| November 13, 2015 | K152936 | Sirius Max Dental Diode Curing Light | EBZ | Substantially Equivalent | National Dental, Inc. | accessdata.fda.gov |
| April 24, 2015 | K141482 | KI-20 | EBW | Substantially Equivalent | Saeyang Microtech Co., Ltd. | accessdata.fda.gov |
| April 24, 2014 | K133007 | DX3000-L | MUH | Substantially Equivalent | Dexcowin Co., Ltd. | accessdata.fda.gov |
| March 28, 2014 | K133170 | QUICK JET M | EFB | Substantially Equivalent | Micron Corp. | accessdata.fda.gov |
| December 7, 2012 | K122582 | DENTAL X-RAY Z70 (W); DENTAL X-RAY Z70 (M); DENTAL X-RAY Z70 (C) | EHD | Substantially Equivalent | Denterprise International, Inc. | accessdata.fda.gov |
| December 16, 2009 | K093084 | ROLENCE DENTAL HIGH SPEED HANDPIECE, RHP | EFB | Substantially Equivalent | Rolence Ent., Inc. | accessdata.fda.gov |
| January 25, 2007 | K070155 | INTEGRITY LOW SPEED DENTAL AIR HANDPIECE AND ATTACHMENT, MODELS: MOTOR INT-E, MOTOR INT-D AND ATTACHMENT INT-SNC | EFB | Substantially Equivalent | Osseo Scientific, LLC | accessdata.fda.gov |
| October 3, 2005 | K051872 | MK-DENT LOW SPEED HANDPIECES AND ACCESSORIES INCLUDING SPARE PARTS, TUBINGS, AND LIGHT POWER SYSTEM, MODELS: LS2011 | EFB | Substantially Equivalent | Mk-Dent GmbH | accessdata.fda.gov |
| April 22, 2004 | K040396 | ULTRASONIC SCALER ELEGANCE MS-10 (25K) | ELC | Substantially Equivalent | Rolence Enteprise, Inc. | accessdata.fda.gov |
| November 20, 2003 | K032995 | SSS, MODEL 1072001 (STANDARD 4-HOLE MODEL) & 1072002 (STANDARD 2-HOLE MODEL) | ELC | Substantially Equivalent | Micron Corp. | accessdata.fda.gov |
| October 2, 2003 | K032234 | MK-DENT HIGH SPEED DENTAL HANDPIECE, MODELS HS 4021K, 4011K, 4012K, AND HS 6021K, 6011K, 6012K | EFB | Substantially Equivalent | Mk-Dent GmbH | accessdata.fda.gov |
| December 30, 2002 | K023545 | ULTRA-LITE 200E LIGHT CURE UNIT | EBZ | Substantially Equivalent | Rolence Ent., Inc. | accessdata.fda.gov |
| October 22, 2002 | K022535 | MICROTECH PUSH BUTTON HANDPIECE, MODEL MHS-A100 | EFB | Substantially Equivalent | Microtech | accessdata.fda.gov |
| October 10, 2000 | K001719 | Q-LUX PLASMA 100 LIGHT CURE UNIT | EBZ | Substantially Equivalent | Rolence Enterprise Co. , Ltd. | accessdata.fda.gov |
| April 15, 1996 | K960351 | Q-LUX LIGHT CURE UNIT | EBZ | Substantially Equivalent | Rolence Enterprise Co. , Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Handpiece, Air-Powered, Dental
- All makers of Activator, Ultraviolet, For Polymerization
- All makers of Unit, X-Ray, Extraoral With Timer
- All makers of Scaler, Ultrasonic
- All makers of Sterilizer, Steam
- All makers of Controller, Foot, Handpiece And Cord
Updated February 22, 2022. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.