TRAUS Air Dental Handpiece

FDA 510(k) K221741 · Saeshin Precision Co., Ltd.

Substantially Equivalent

510(k) numberK221741

Submission

Device name
TRAUS Air Dental Handpiece
Applicant
Saeshin Precision Co., Ltd.
Daegu, KR
Received
June 15, 2022
Decision date
February 22, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EFB – Handpiece, Air-Powered, Dental
Device class
Class I (low risk)
Regulation
21 CFR 872.4200
Specialty
Dental

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Questions and answers

When was TRAUS Air Dental Handpiece cleared by the FDA?

TRAUS Air Dental Handpiece (K221741) received a 510(k) decision of Substantially Equivalent on February 22, 2023, 252 days after the submission was received.

What is the product code of K221741?

The FDA product code is EFB – Handpiece, Air-Powered, Dental, a Class I (low risk) device regulated under 21 CFR 872.4200.