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FDA 510(k)

Jason membrane

K-Number: K242817 · 2025-12-12

ApplicantBotiss Biomaterials GmbH
Decision Date2025-12-12
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Jason membrane is a medical device manufactured by Botiss Biomaterials GmbH. It received FDA 510(k) clearance on 2025-12-12 under approval number K242817. The device is classified under product code NPL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Jason membrane?

Jason membrane is a medical device that received FDA 510(k) clearance on 2025-12-12. It is manufactured by Botiss Biomaterials GmbH. The 510(k) number is K242817.

When was Jason membrane approved by the FDA?

Jason membrane received FDA 510(k) clearance on 2025-12-12, under approval number K242817.

What company makes Jason membrane?

Jason membrane is manufactured by Botiss Biomaterials GmbH.

What is the FDA product code for Jason membrane?

The FDA product code for Jason membrane is NPL.

Related Clinical Trials

NCT06059898 Magnesium NOVAMag® Membrane vs. Collagen Jason® Membrane in Patients Requiring Guided Bone Regeneration COMPLETED

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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.

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