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FDA 510(k)

V-Print dentbase

K-Number: K220236 · 2022-09-21

ApplicantVoco GmbH
Decision Date2022-09-21
Product CodeEBI
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

V-Print dentbase is a medical device manufactured by Voco GmbH. It received FDA 510(k) clearance on 2022-09-21 under approval number K220236. The device is classified under product code EBI. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-Print dentbase?

V-Print dentbase is a medical device that received FDA 510(k) clearance on 2022-09-21. It is manufactured by Voco GmbH. The 510(k) number is K220236.

When was V-Print dentbase approved by the FDA?

V-Print dentbase received FDA 510(k) clearance on 2022-09-21, under approval number K220236.

What company makes V-Print dentbase?

V-Print dentbase is manufactured by Voco GmbH.

What is the FDA product code for V-Print dentbase?

The FDA product code for V-Print dentbase is EBI.

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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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