V-Print dentbase
K-Number: K220236 · 2022-09-21
Device Summary
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. The listed applicant is Voco GmbH. The 510(k) number is K220236.
When did V-Print dentbase receive FDA 510(k) clearance?
V-Print dentbase received FDA 510(k) clearance on 2022-09-21, under 510(k) number K220236.
Who is the listed applicant for V-Print dentbase?
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 dentbase?
The FDA product code for V-Print dentbase is EBI.
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.
Related Devices (Code: EBI)
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.
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.