Geistlich Pharma AG - FDA 510(k) Cleared Devices
Recent clearances: Device 300419 Strip, Derma-Gide, Device 104 Particulate
27
Total
27
Cleared
0
Denied
FDA 510(k) Regulatory Record - Geistlich Pharma AG General & Plastic Surgery ✕
6 devices
Cleared
Mar 19, 2026
Derma-Gide
General & Plastic Surgery
30d
Cleared
Jan 22, 2026
Device 104 Particulate
General & Plastic Surgery
268d
Cleared
Apr 28, 2022
Geistlich Wound Matrix PLUS
General & Plastic Surgery
164d
Cleared
Jul 14, 2021
Nexo-Gide Bilayer Collagen Membrane
General & Plastic Surgery
229d
Cleared
Nov 08, 2018
Geistlich Derma-Gide
General & Plastic Surgery
30d
Cleared
Nov 03, 2017
Geistlich Wound Matrix
General & Plastic Surgery
136d