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FDA 510(k)

FREEPRINT crown

K-Number: K222877 · 2022-09-23

ApplicantDetax GmbH
Decision Date2022-09-23
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FREEPRINT crown is a medical device manufactured by Detax GmbH. It received FDA 510(k) clearance on 2022-09-23 under approval number K222877. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FREEPRINT crown?

FREEPRINT crown is a medical device that received FDA 510(k) clearance on 2022-09-23. It is manufactured by Detax GmbH. The 510(k) number is K222877.

When was FREEPRINT crown approved by the FDA?

FREEPRINT crown received FDA 510(k) clearance on 2022-09-23, under approval number K222877.

What company makes FREEPRINT crown?

FREEPRINT crown is manufactured by Detax GmbH.

What is the FDA product code for FREEPRINT crown?

The FDA product code for FREEPRINT crown is EBF.

Other Devices by Detax GmbH

K232448FREEPRINT® splintmaster K252430Freeprint® denture flex

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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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