Dental unit Model: Mare

FDA 510(k) K231845 · Foshan Safety Medical Equipment Co., Ltd.

Substantially Equivalent

510(k) numberK231845

Submission

Device name
Dental unit Model: Mare
Applicant
Foshan Safety Medical Equipment Co., Ltd.
Foshan, CN
Received
June 22, 2023
Decision date
February 28, 2024
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EIA – Unit, Operative Dental
Device class
Class I (low risk)
Regulation
21 CFR 872.6640
Specialty
Dental

Other 510(k)s with product code EIA

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K251626Midmark Dental Delivery SystemEIA · Traditional Midmark Corporation11/03/2025SE
K251491K5 Cart, K5 Mount, K5 SwingEIA · Special Osstem Implant Company., Ltd. Chair Business07/17/2025SE
K243130Integral Dental UnitEIA · Traditional Guangdong Yadeng Medical Apparatus Co., Ltd.,06/27/2025SE
K242611Integral Dental UnitsEIA · Traditional Mipont Medical Equipment Co., Ltd.05/27/2025SE
K250473Dental Delivery System Series 5 and Dental Delivery System Series 5 PlusEIA · Traditional Dci International, LLC02/19/2025SE
K242404BDC Dental UnitEIA · Traditional Bdc Dental Corporation , Ltd.02/07/2025SE
K231297Firstar Dental UnitEIA · Traditional Firstar Dental Company01/27/2025SE
K233805K5EIA · Traditional Osstem Implant Co., Ltd. Chair Business09/03/2024SE
K240754N2EIA · Special Megagen Implant Co., Ltd.03/21/2024SE

Questions and answers

When was Dental unit Model: Mare cleared by the FDA?

Dental unit Model: Mare (K231845) received a 510(k) decision of Substantially Equivalent on February 28, 2024, 251 days after the submission was received.

What is the product code of K231845?

The FDA product code is EIA – Unit, Operative Dental, a Class I (low risk) device regulated under 21 CFR 872.6640.