ClearCorrect System
K-Number: K220140 · 2022-10-05
ApplicantClearcorrect, LLC
Decision Date2022-10-05
Product CodeNXC
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
ClearCorrect System is a medical device manufactured by Clearcorrect, LLC. It received FDA 510(k) clearance on 2022-10-05 under approval number K220140. 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 ClearCorrect System?
ClearCorrect System is a medical device that received FDA 510(k) clearance on 2022-10-05. It is manufactured by Clearcorrect, LLC. The 510(k) number is K220140.
When was ClearCorrect System approved by the FDA?
ClearCorrect System received FDA 510(k) clearance on 2022-10-05, under approval number K220140.
What company makes ClearCorrect System?
ClearCorrect System is manufactured by Clearcorrect, LLC.
What is the FDA product code for ClearCorrect System?
The FDA product code for ClearCorrect System is NXC.
Other Devices by Clearcorrect, LLC
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.