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 a medical device manufactured by Kavo Dental Technologies, LLC. It received FDA 510(k) clearance on 2017-12-18 under approval 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. It is manufactured by Kavo Dental Technologies, LLC. The 510(k) number is K172918.
When was DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) approved by the FDA?
DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) received FDA 510(k) clearance on 2017-12-18, under approval number K172918.
What company makes DEXIS Titanium, KaVo IXS HD (Size 1, Size 2)?
DEXIS Titanium, KaVo IXS HD (Size 1, Size 2) is manufactured by Kavo Dental Technologies, LLC.
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)
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.