FDA 510(k)

Ivotion Base Print

K-Number: K233995 · 2024-02-23

Decision Date2024-02-23

Product CodeEBI

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

Ivotion Base Print is a medical device manufactured by Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2024-02-23 under approval number K233995. 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 Ivotion Base Print?

Ivotion Base Print is a medical device that received FDA 510(k) clearance on 2024-02-23. It is manufactured by Ivoclar Vivadent, Inc.. The 510(k) number is K233995.

When was Ivotion Base Print approved by the FDA?

Ivotion Base Print received FDA 510(k) clearance on 2024-02-23, under approval number K233995.

What company makes Ivotion Base Print?

Ivotion Base Print is manufactured by Ivoclar Vivadent, Inc..

What is the FDA product code for Ivotion Base Print?

The FDA product code for Ivotion Base Print is EBI.

Other Devices by Ivoclar Vivadent, Inc.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.