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FDA 510(k)

ENDOSEAL MTA

K-Number: K170175 · 2018-02-26

ApplicantMaruchi
Decision Date2018-02-26
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ENDOSEAL MTA is a medical device manufactured by Maruchi. It received FDA 510(k) clearance on 2018-02-26 under approval number K170175. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSEAL MTA?

ENDOSEAL MTA is a medical device that received FDA 510(k) clearance on 2018-02-26. It is manufactured by Maruchi. The 510(k) number is K170175.

When was ENDOSEAL MTA approved by the FDA?

ENDOSEAL MTA received FDA 510(k) clearance on 2018-02-26, under approval number K170175.

What company makes ENDOSEAL MTA?

ENDOSEAL MTA is manufactured by Maruchi.

What is the FDA product code for ENDOSEAL MTA?

The FDA product code for ENDOSEAL MTA is KIF.

Other Devices by Maruchi

K212229White Endoseal MTA K202015White ENDOSEAL MTA K201799CleaniCal K213757Endocem MTA Premixed Regular

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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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