Skip to content

dentona flexisplint, optimill memosplint, dentona vivatemp, optimill memosplint version S

by dentona AG

510(k) K222604

Listed No authorization on record

Valid until

Not applicable

No authorization on record

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 6 Oct 2026. What this means

Specification

510(k)

510(k) Number
FDA Product Code
MQC
Device Class
U
Advisory Committee
Unknown
FDA Decision
SESE Substantially Equivalent

Other devices from dentona AG

See all devices from dentona AG →