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FDA 510(k)

SwissMembrane X; SwissMembrane X Socket

K-Number: K250833 · 2025-04-15

ApplicantGeistlich Pharma AG
Decision Date2025-04-15
Product CodeNPL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SwissMembrane X; SwissMembrane X Socket is a medical device manufactured by Geistlich Pharma AG. It received FDA 510(k) clearance on 2025-04-15 under approval number K250833. 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 SwissMembrane X; SwissMembrane X Socket?

SwissMembrane X; SwissMembrane X Socket is a medical device that received FDA 510(k) clearance on 2025-04-15. It is manufactured by Geistlich Pharma AG. The 510(k) number is K250833.

When was SwissMembrane X; SwissMembrane X Socket approved by the FDA?

SwissMembrane X; SwissMembrane X Socket received FDA 510(k) clearance on 2025-04-15, under approval number K250833.

What company makes SwissMembrane X; SwissMembrane X Socket?

SwissMembrane X; SwissMembrane X Socket is manufactured by Geistlich Pharma AG.

What is the FDA product code for SwissMembrane X; SwissMembrane X Socket?

The FDA product code for SwissMembrane X; SwissMembrane X Socket is NPL.

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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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