Not currently registered with FDA under this name
Ed. Geistlich Soehne AG Fuer Chemische Industrie
Washington, DC, United States. Named as applicant on 6 dental 510(k) clearances between 2003 and 2010. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 62003–2010
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Ed. Geistlich Soehne AG Fuer Chemische Industrie as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 18 Mar 2010 | K092428 | BIO-OSS COLLAGEN | NPM Animal Source Bone Grafting Material |
| 30 May 2008 | K073711 | MUCOGRAFT COLLAGEN MATRIX | NPL Intraoral Animal Source Barrier |
| 6 Jun 2006 | K061244 | MUCOGRAFT | NPL Intraoral Animal Source Barrier |
| 9 Aug 2005 | K050446 | BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE | NPL Intraoral Animal Source Barrier |
| 15 Nov 2004 | K042197 | BIO-GIDE RESORBABLE BILAYER MEMBRANE FOR GUIDED TISSUE AND BONE REGENERATION | NPL Intraoral Animal Source Barrier |
| 24 Jan 2003 | K012423 | MUCOGRAFT | NPL Intraoral Animal Source Barrier |
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.