Bright Temporary C&B
K-Number: K192830 · 2020-09-02
ApplicantDmp Dental Industry S.A.
Decision Date2020-09-02
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Bright Temporary C&B is a medical device manufactured by Dmp Dental Industry S.A.. It received FDA 510(k) clearance on 2020-09-02 under approval 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. It is manufactured by Dmp Dental Industry S.A.. The 510(k) number is K192830.
When was Bright Temporary C&B approved by the FDA?
Bright Temporary C&B received FDA 510(k) clearance on 2020-09-02, under approval number K192830.
What company makes Bright Temporary C&B?
Bright Temporary C&B is manufactured by Dmp Dental Industry S.A..
What is the FDA product code for Bright Temporary C&B?
The FDA product code for Bright Temporary C&B is EBG.
Other Devices by Dmp Dental Industry S.A.
Related Devices (Code: EBG)
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.