Medical Device Manufacturer · US , Washington , DC

Geistlich Pharma AG - FDA 510(k) Cleared Devices

27 submissions · 27 cleared · Since 2011

Recent clearances: Device 300419 Strip, Derma-Gide, Device 104 Particulate

Total

Cleared

Denied

Geistlich Pharma AG has 27 FDA 510(k) cleared medical devices. Based in Washington, US.

Latest FDA clearance: Jun 2026. Active since 2011. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Geistlich Pharma AG Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Telos Partners, LLC, QUARAS, LLC and Streamline Regulatory.

Geistlich Pharma AG is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Geistlich Pharma AG

27 devices

1-12 of 27

General & Plastic Surgery · 30d

Cleared Jan 22, 2026

Device 104 Particulate

K251323 · KGN

General & Plastic Surgery · 268d

Cleared Nov 25, 2025

Geistlich Mucograft® /Geistlich Mucograft® Seal

Device 300423 Granules

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Jun 08, 2026

Geistlich Pharma AG - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Geistlich Pharma AG

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