The POD
K-Number: K182820 · 2019-07-17
ApplicantAdvanced Facialdontics, LLC
Decision Date2019-07-17
Product CodeMQC
DecisionSubstantially Equivalent
Device Summary
The POD is a medical device manufactured by Advanced Facialdontics, LLC. It received FDA 510(k) clearance on 2019-07-17 under approval number K182820. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the The POD?
The POD is a medical device that received FDA 510(k) clearance on 2019-07-17. It is manufactured by Advanced Facialdontics, LLC. The 510(k) number is K182820.
When was The POD approved by the FDA?
The POD received FDA 510(k) clearance on 2019-07-17, under approval number K182820.
What company makes The POD?
The POD is manufactured by Advanced Facialdontics, LLC.
What is the FDA product code for The POD?
The FDA product code for The POD is MQC.
Other Devices by Advanced Facialdontics, LLC
Related Devices (Code: MQC)
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.