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. The listed applicant is Dentona AG. The 510(k) number is K222604.
When did dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S receive FDA 510(k) clearance?
dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S received FDA 510(k) clearance on 2023-04-21, under 510(k) number K222604.
Who is the listed applicant for dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S?
The FDA 510(k) record lists Dentona AG as the applicant. This does not by itself establish the device manufacturer.
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)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
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