FDA 510(k)

Ti-Base & Master Fix

K-Number: K240603 · 2024-06-05

Decision Date2024-06-05

Product CodeNHA

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Ti-Base & Master Fix is a medical device manufactured by Arum Dentistry Co., Ltd.. It received FDA 510(k) clearance on 2024-06-05 under approval number K240603. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Ti-Base & Master Fix?

Ti-Base & Master Fix is a medical device that received FDA 510(k) clearance on 2024-06-05. It is manufactured by Arum Dentistry Co., Ltd.. The 510(k) number is K240603.

When was Ti-Base & Master Fix approved by the FDA?

Ti-Base & Master Fix received FDA 510(k) clearance on 2024-06-05, under approval number K240603.

What company makes Ti-Base & Master Fix?

Ti-Base & Master Fix is manufactured by Arum Dentistry Co., Ltd..

What is the FDA product code for Ti-Base & Master Fix?

The FDA product code for Ti-Base & Master Fix is NHA.

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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.