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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 a medical device manufactured by Vita Zahnfabrik GmbH H Rauter & CO. It received FDA 510(k) clearance on 2021-11-22 under approval 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. It is manufactured by Vita Zahnfabrik GmbH H Rauter & CO. The 510(k) number is K211854.

When was VITA Akzent LC approved by the FDA?

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

What company makes VITA Akzent LC?

VITA Akzent LC is manufactured by Vita Zahnfabrik GmbH H Rauter & CO.

What is the FDA product code for VITA Akzent LC?

The FDA product code for VITA Akzent LC is EBD.

Other Devices by Vita Zahnfabrik GmbH H Rauter & CO

K193434VITA LUMEX AC K193436VITA Ambria

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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.

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