Geistlich Pharma AG - FDA 510(k) Cleared Devices
26
Total
26
Cleared
0
Denied
Geistlich Pharma AG has 26 FDA 510(k) cleared medical devices. Based in Washington, US.
Latest FDA clearance: Mar 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.
FDA 510(k) cleared devices by Geistlich Pharma AG
26 devices
Cleared
Mar 19, 2026
Derma-Gide
General & Plastic Surgery
30d
Cleared
Jan 22, 2026
Device 104 Particulate
General & Plastic Surgery
268d
Cleared
Nov 25, 2025
Geistlich Mucograft® /Geistlich Mucograft® Seal
Dental
127d
Cleared
Aug 14, 2025
Geistlich Bio-Gide
Dental
132d
Cleared
Jul 17, 2025
Device 300423 Granules
Orthopedic
57d
Cleared
Jul 11, 2025
Geistlich Bio-Oss®
Dental
30d
Cleared
Jun 26, 2025
SwissGraft X
Dental
30d
Cleared
Apr 15, 2025
SwissMembrane X
Dental
27d
Cleared
Mar 07, 2025
Geistlich Bio-Flow®
Dental
196d
Cleared
Nov 08, 2024
Device 300397 Putty
Orthopedic
140d
Cleared
Jul 12, 2024
Geistlich Bio-Oss®
Dental
126d
Cleared
Apr 28, 2022
Geistlich Wound Matrix PLUS
General & Plastic Surgery
164d