Copran Zri
K-Number: K232952 · 2024-06-24
ApplicantWhitepeaks Dental Solutions GmbH
Decision Date2024-06-24
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Copran Zri is a medical device manufactured by Whitepeaks Dental Solutions GmbH. It received FDA 510(k) clearance on 2024-06-24 under approval number K232952. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Copran Zri?
Copran Zri is a medical device that received FDA 510(k) clearance on 2024-06-24. It is manufactured by Whitepeaks Dental Solutions GmbH. The 510(k) number is K232952.
When was Copran Zri approved by the FDA?
Copran Zri received FDA 510(k) clearance on 2024-06-24, under approval number K232952.
What company makes Copran Zri?
Copran Zri is manufactured by Whitepeaks Dental Solutions GmbH.
What is the FDA product code for Copran Zri?
The FDA product code for Copran Zri is EIH.
Other Devices by Whitepeaks Dental Solutions GmbH
Related Devices (Code: EIH)
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.