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FDA 510(k)

Bright Temporary C&B

K-Number: K192830 · 2020-09-02

Decision Date2020-09-02
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Bright Temporary C&B is the device name listed in this FDA 510(k) record. The listed applicant is Dmp Dental Industry S.A.. It received FDA 510(k) clearance on 2020-09-02 under 510(k) number K192830. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Bright Temporary C&B?

Bright Temporary C&B is a medical device that received FDA 510(k) clearance on 2020-09-02. The listed applicant is Dmp Dental Industry S.A.. The 510(k) number is K192830.

When did Bright Temporary C&B receive FDA 510(k) clearance?

Bright Temporary C&B received FDA 510(k) clearance on 2020-09-02, under 510(k) number K192830.

Who is the listed applicant for Bright Temporary C&B?

The FDA 510(k) record lists Dmp Dental Industry S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Bright Temporary C&B?

The FDA product code for Bright Temporary C&B is EBG.

Other records listing Dmp Dental Industry S.A. 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: EBG)

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.