Class Class II

Jason membrane (K242817)

K242817 2025-12-12 Traditional
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Description

Jason membrane by Botiss Biomaterials GmbH, an FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242817
Clearance Date2025-12-12
Clearance TypeTraditional
Product CodeNPL
Regulation Number872.3930

Categories

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