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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Vita Zahnfabrik H.Rauter GmbH & Co.. It received FDA 510(k) clearance on 2025-02-21 under 510(k) 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. The listed applicant is Vita Zahnfabrik H.Rauter GmbH & Co.. The 510(k) number is K243940.

When did VITA YZ Multi Translucent receive FDA 510(k) clearance?

VITA YZ Multi Translucent received FDA 510(k) clearance on 2025-02-21, under 510(k) number K243940.

Who is the listed applicant for VITA YZ Multi Translucent?

The FDA 510(k) record lists Vita Zahnfabrik H.Rauter GmbH & Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITA YZ Multi Translucent?

The FDA product code for VITA YZ Multi Translucent is EIH.

Other records listing Vita Zahnfabrik H.Rauter GmbH & Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K180703VITA YZ ST and VITA YZ XTK153645VITA ENAMIC Implant Solutions (IS)

Related Devices (Code: EIH)

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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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