Overjet Periapical Radiolucency Assist
K-Number: K231678 · 2023-09-21
ApplicantOverjet, Inc.
Decision Date2023-09-21
Product CodeMYN
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
Overjet Periapical Radiolucency Assist is a medical device manufactured by Overjet, Inc.. It received FDA 510(k) clearance on 2023-09-21 under approval number K231678. The device is classified under product code MYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Overjet Periapical Radiolucency Assist?
Overjet Periapical Radiolucency Assist is a medical device that received FDA 510(k) clearance on 2023-09-21. It is manufactured by Overjet, Inc.. The 510(k) number is K231678.
When was Overjet Periapical Radiolucency Assist approved by the FDA?
Overjet Periapical Radiolucency Assist received FDA 510(k) clearance on 2023-09-21, under approval number K231678.
What company makes Overjet Periapical Radiolucency Assist?
Overjet Periapical Radiolucency Assist is manufactured by Overjet, Inc..
What is the FDA product code for Overjet Periapical Radiolucency Assist?
The FDA product code for Overjet Periapical Radiolucency Assist is MYN.
Other Devices by Overjet, Inc.
Related Devices (Code: MYN)
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.