Concinnity Aligners
K-Number: K200005 · 2020-11-09
Decision Date2020-11-09
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Concinnity Aligners is a medical device manufactured by Drake Precision Dental Laboratory, Inc.. It received FDA 510(k) clearance on 2020-11-09 under approval number K200005. The device is classified under product code NXC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Concinnity Aligners?
Concinnity Aligners is a medical device that received FDA 510(k) clearance on 2020-11-09. It is manufactured by Drake Precision Dental Laboratory, Inc.. The 510(k) number is K200005.
When was Concinnity Aligners approved by the FDA?
Concinnity Aligners received FDA 510(k) clearance on 2020-11-09, under approval number K200005.
What company makes Concinnity Aligners?
Concinnity Aligners is manufactured by Drake Precision Dental Laboratory, Inc..
What is the FDA product code for Concinnity Aligners?
The FDA product code for Concinnity Aligners is NXC.
Related Devices (Code: NXC)
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.