Not currently registered with FDA under this name
Depuy, Inc.
Warsaw, IN, United States. Named as applicant on 5 dental 510(k) clearances between 1977 and 1987. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51977–1987
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1976–2026
510(k) clearances
Clearances on which FDA names Depuy, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 4 Jun 1987 | K871219 | TITANODONT SUBCORTICAL IMPLANT WITH POROCOAT | DZE Root-Form Endosseous Implant |
| 7 Nov 1984 | K842718 | HYDROXYAPATITE | LYC Synthetic Bone Grafting Material |
| 12 Aug 1982 | K821752 | SYNTHOGRAFT LG-AUGMENTATION & BONE FILL | LYC Synthetic Bone Grafting Material |
| 28 Sep 1979 | K791204 | MITER ENDOSTEAL BLADE IMPLANT | NRQ Blade-Form Endosseous Dental Implant |
| 28 Sep 1977 | K771747 | PERIOSTEAL ELEVATOR | EMJ Dental Surgical Elevator |
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.