Vector R&D, Inc VKS

• FDA 510(k) K051872 decided 3 Oct 2005 Active
• FDA GUDID UDI-DI 00810113690254 listed 30 Sep 2022 Listed

1. 3 Oct 2005 Cleared FDA 510(k) K051872
2. 30 Sep 2022 Listed FDA GUDID 00810113690254

Trade name

Vector R&D, Inc

Generic name

Pneumatic dental handpiece coupler

Model / Ref / Catalog

VKS

Primary DI / UDI-DI

00810113690254

510(k) Number

K051872 ↗

FDA product code

EFB

GMDN term

Pneumatic dental handpiece coupler

Device class

Class I

Regulation number

872.4200

GUDID distribution status

In Commercial Distribution

MRI safety

MR Unsafe

Category: Pneumatic dental handpiece coupler

Other devices filed under FDA product code EFB (Handpiece, air-powered, dental).

• Dental Handpiece (Model: J6-126, J6-136, SH11W2, SH11W3, W401LW, W15LW, W142LW, W11L) by Guangdong JINME Medical Technology Co., Ltd.
• AIR-FLOW HANDY 3.0 by E.M.S. Electro Medical Systems S.A.
• CARE3 PLUS by NAKANISHI INC.
• AUTOCHUCK ATTACHMENT by Den-Tal-Ez Mfg Co., Inc.
• PACEMAKER HIGH-SPEED HANDPIECE MODEL PM-MQ, PM-M by Delma Medical Instrument (Guangzhou) Co., Ltd.
• SIROAIR L AIR SCALER by SIRONA Dental Systems GmbH
• LC COMPOSITE by Harry J. Bosworth Co.
• PLAQUE-SWEEP by Dentsply Intl.
• EMS AIR-FLOW MASTER by E.M.S. Electro Medical Systems S.A.
• MACH-SIGMA HANDPIECE, ULTRAPUSH by Nsk Nakanishi, Inc.

• Vector R&D, Inc DRA-NK

  Class I

  FDA 510(k) K051872 Active Cleared 3 Oct 2005 GUDID on market

• Vector R&D, Inc F4

  Class I

  FDA 510(k) K032234 Active Cleared 2 Oct 2003 GUDID on market

• Vector R&D, Inc VM25LPA

  Class I

  FDA 510(k) K051872 Active Cleared 3 Oct 2005 GUDID on market

• Vector R&D, Inc KV80

  Class I

  FDA 510(k) K051872 Active Cleared 3 Oct 2005 GUDID on market

See all devices from Vector R&D, Inc. →