Not currently registered with FDA under this name
Driskell Bioengineering
Galena, OH, United States. Named as applicant on 4 dental 510(k) clearances between 1985 and 1988. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 41985–1988
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1980–2026
510(k) clearances
Clearances on which FDA names Driskell Bioengineering as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 26 Feb 1988 | K875243 | DB PRECISION IMPLANT SYSTEM, 2000 SERIES W/HAC | DZE Root-Form Endosseous Implant |
| 26 Feb 1988 | K875242 | DB PRECISION IMPLANT SYSTEM, 1000 SERIES W/HAC | DZE Root-Form Endosseous Implant |
| 25 Apr 1986 | K860982 | DB PRECISION IMPLANT SYSTEM, 2000 SERIES | DZE Root-Form Endosseous Implant |
| 31 Oct 1985 | K853788 | DB PRECISION IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: Bicon, LLC (1).
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.