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FDA 510(k)

VITA Akzent LC

K-Number: K211854 · 2021-11-22

ApplicantVita Zahnfabrik GmbH H Rauter & CO
Decision Date2021-11-22
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VITA Akzent LC is the device name listed in this FDA 510(k) record. The listed applicant is Vita Zahnfabrik GmbH H Rauter & CO. It received FDA 510(k) clearance on 2021-11-22 under 510(k) number K211854. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITA Akzent LC?

VITA Akzent LC is a medical device that received FDA 510(k) clearance on 2021-11-22. The listed applicant is Vita Zahnfabrik GmbH H Rauter & CO. The 510(k) number is K211854.

When did VITA Akzent LC receive FDA 510(k) clearance?

VITA Akzent LC received FDA 510(k) clearance on 2021-11-22, under 510(k) number K211854.

Who is the listed applicant for VITA Akzent LC?

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

What is the FDA product code for VITA Akzent LC?

The FDA product code for VITA Akzent LC is EBD.

Other records listing Vita Zahnfabrik GmbH H Rauter & 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.

K193434VITA LUMEX ACK193436VITA Ambria

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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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