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FDA 510(k)

DEXIS Titanium, KaVo IXS HD (Size 1, Size 2)

K-Number: K172918 · 2017-12-18

ApplicantKavo Dental Technologies, LLC
Decision Date2017-12-18
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) is the device name listed in this FDA 510(k) record. The listed applicant is Kavo Dental Technologies, LLC. It received FDA 510(k) clearance on 2017-12-18 under 510(k) number K172918. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEXIS Titanium, KaVo IXS HD (Size 1, Size 2)?

DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) is a medical device that received FDA 510(k) clearance on 2017-12-18. The listed applicant is Kavo Dental Technologies, LLC. The 510(k) number is K172918.

When did DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) receive FDA 510(k) clearance?

DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) received FDA 510(k) clearance on 2017-12-18, under 510(k) number K172918.

Who is the listed applicant for DEXIS Titanium, KaVo IXS HD (Size 1, Size 2)?

The FDA 510(k) record lists Kavo Dental Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DEXIS Titanium, KaVo IXS HD (Size 1, Size 2)?

The FDA product code for DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) is MUH.

Related Devices (Code: MUH)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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