Bright Temporary C&B
K-Number: K192830 · 2020-09-02
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.