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FDA 510(k)

BruxZir™ Incisal Coloring Liquid

K-Number: K230262 · 2023-05-16

Decision Date2023-05-16
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BruxZir™ Incisal Coloring Liquid is the device name listed in this FDA 510(k) record. The listed applicant is Prismatik Dentalcraft, Inc.. It received FDA 510(k) clearance on 2023-05-16 under 510(k) number K230262. 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 BruxZir™ Incisal Coloring Liquid?

BruxZir™ Incisal Coloring Liquid is a medical device that received FDA 510(k) clearance on 2023-05-16. The listed applicant is Prismatik Dentalcraft, Inc.. The 510(k) number is K230262.

When did BruxZir™ Incisal Coloring Liquid receive FDA 510(k) clearance?

BruxZir™ Incisal Coloring Liquid received FDA 510(k) clearance on 2023-05-16, under 510(k) number K230262.

Who is the listed applicant for BruxZir™ Incisal Coloring Liquid?

The FDA 510(k) record lists Prismatik Dentalcraft, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BruxZir™ Incisal Coloring Liquid?

The FDA product code for BruxZir™ Incisal Coloring Liquid is EIH.

Other records listing Prismatik Dentalcraft, Inc. 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.

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Related Devices (Code: EIH)

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

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