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FDA 510(k)

Dental Low-speed Handpieces and Accessories

K-Number: K202786 · 2021-09-03

ApplicantMicrop Technology (Taiwan), Inc.
Decision Date2021-09-03
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Dental Low-speed Handpieces and Accessories is a medical device manufactured by Microp Technology (Taiwan), Inc.. It received FDA 510(k) clearance on 2021-09-03 under approval number K202786. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dental Low-speed Handpieces and Accessories?

Dental Low-speed Handpieces and Accessories is a medical device that received FDA 510(k) clearance on 2021-09-03. It is manufactured by Microp Technology (Taiwan), Inc.. The 510(k) number is K202786.

When was Dental Low-speed Handpieces and Accessories approved by the FDA?

Dental Low-speed Handpieces and Accessories received FDA 510(k) clearance on 2021-09-03, under approval number K202786.

What company makes Dental Low-speed Handpieces and Accessories?

Dental Low-speed Handpieces and Accessories is manufactured by Microp Technology (Taiwan), Inc..

What is the FDA product code for Dental Low-speed Handpieces and Accessories?

The FDA product code for Dental Low-speed Handpieces and Accessories is EFB.

Other Devices by Microp Technology (Taiwan), Inc.

K173943Dental High-speed Handpiece and Accessories

Related Devices (Code: EFB)

K160410WOlf High Speed Handpieces - Medium head, WOlf High Speed Handpieces - Small headDental Savings Club K153411430 Torque High-Speed Handpiece Series - 430 SWL Torque High Speed Handpiece, 430 SW Torque High Speed HandpieceDentalez, Inc. K151912AIR-FLOW handy 3.0 PLUSE.M.S Electro Medical Systems S.A K171174PERIO-FLOW nozzleE.M.S Electro Medical Systems S.A K171553W&H Assistina TwinW&H Dentalwerk Buermoos GmbH K170236Dental Low-speed Turbine HandpieceGuangdong Jinme Medical Technology Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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