FDA 510(k)

V-Print c&b temp

K-Number: K231591 · 2023-07-31

Decision Date2023-07-31

Product CodePOW

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

V-Print c&b temp is the device name listed in this FDA 510(k) record. The listed applicant is Voco GmbH. It received FDA 510(k) clearance on 2023-07-31 under 510(k) number K231591. The device is classified under product code POW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V-Print c&b temp?

V-Print c&b temp is a medical device that received FDA 510(k) clearance on 2023-07-31. The listed applicant is Voco GmbH. The 510(k) number is K231591.

When did V-Print c&b temp receive FDA 510(k) clearance?

V-Print c&b temp received FDA 510(k) clearance on 2023-07-31, under 510(k) number K231591.

Who is the listed applicant for V-Print c&b temp?

The FDA 510(k) record lists Voco GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-Print c&b temp?

The FDA product code for V-Print c&b temp is POW.

Other records listing Voco GmbH 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.

K252073VOCO Profluorid Varnish + BioMin K261357Grandio disc multicolor K252606Bifix Veneer LC, Bifix Veneer Try-In K251390MTA vpt K251239GrandioSO Unlimited K231817AlignerFlow LC

View all 29 devices →

Related Devices (Code: POW)

K261456Ruthinium DiscDental Manufacturing S.p.A.

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.