VITA YZ Multi Translucent
K-Number: K243940 · 2025-02-21
ApplicantVita Zahnfabrik H.Rauter GmbH & Co.
Decision Date2025-02-21
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
VITA YZ Multi Translucent is a medical device manufactured by Vita Zahnfabrik H.Rauter GmbH & Co.. It received FDA 510(k) clearance on 2025-02-21 under approval number K243940. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VITA YZ Multi Translucent?
VITA YZ Multi Translucent is a medical device that received FDA 510(k) clearance on 2025-02-21. It is manufactured by Vita Zahnfabrik H.Rauter GmbH & Co.. The 510(k) number is K243940.
When was VITA YZ Multi Translucent approved by the FDA?
VITA YZ Multi Translucent received FDA 510(k) clearance on 2025-02-21, under approval number K243940.
What company makes VITA YZ Multi Translucent?
VITA YZ Multi Translucent is manufactured by Vita Zahnfabrik H.Rauter GmbH & Co..
What is the FDA product code for VITA YZ Multi Translucent?
The FDA product code for VITA YZ Multi Translucent is EIH.
Related Devices (Code: EIH)
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.