dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S
K-Number: K222604 · 2023-04-21
Device Summary
Frequently Asked Questions
What is the dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S?
dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S is a medical device that received FDA 510(k) clearance on 2023-04-21. It is manufactured by Dentona AG. The 510(k) number is K222604.
When was dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S approved by the FDA?
dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S received FDA 510(k) clearance on 2023-04-21, under approval number K222604.
What company makes dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S?
dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S is manufactured by Dentona AG.
What is the FDA product code for dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S?
The FDA product code for dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S is MQC.
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.