Not currently registered with FDA under this name
Osteogenics Co.
Fort Worth, TX, United States. Named as applicant on 2 dental 510(k) clearances between 1997 and 1997. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 21997–1997
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Osteogenics Co. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 6 Aug 1997 | K972278 | CYTOPLAST REGENTEX TITANIUM 250 | LYC Synthetic Bone Grafting Material |
| 11 Mar 1997 | K964342 | CYTOPLAST GBR | LYC Synthetic Bone Grafting Material |
Some of these clearances are listed with FDA today by another company: Dentsply Sirona, Inc. (2), Nobel Biocare Services AG (2), Osteogenics Biomedical, Inc. (2).
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.