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FDA 510(k)

3M Protemp Cement Temporary Dental Cement

K-Number: K170330 · 2017-02-06

Applicant3M Company
Decision Date2017-02-06
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

3M Protemp Cement Temporary Dental Cement is a medical device manufactured by 3M Company. It received FDA 510(k) clearance on 2017-02-06 under approval number K170330. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 3M Protemp Cement Temporary Dental Cement?

3M Protemp Cement Temporary Dental Cement is a medical device that received FDA 510(k) clearance on 2017-02-06. It is manufactured by 3M Company. The 510(k) number is K170330.

When was 3M Protemp Cement Temporary Dental Cement approved by the FDA?

3M Protemp Cement Temporary Dental Cement received FDA 510(k) clearance on 2017-02-06, under approval number K170330.

What company makes 3M Protemp Cement Temporary Dental Cement?

3M Protemp Cement Temporary Dental Cement is manufactured by 3M Company.

What is the FDA product code for 3M Protemp Cement Temporary Dental Cement?

The FDA product code for 3M Protemp Cement Temporary Dental Cement is EMA.

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Related Devices (Code: EMA)

K160800DuoCemColtene/Whaledent AG K161851Glass Ionomer Cement (Luting)Shandong Huge Dental Material Corporation K160443TempoCem ClearDmg USA, Inc. K160774IonoStar PlusVoco GmbH K161256TheraCemBisco, Inc. K153231G-Cem LinkForce, Dual Cure Activator, Try-In Paste, Multi PrimerGC America, Inc.

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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