Not currently registered with FDA under this name
Sargon Ent., Inc.
Washington, DC, United States. Named as applicant on 3 dental 510(k) clearances between 1994 and 2010. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 31994–2010
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Sargon Ent., Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 21 Jul 2010 | K082573 | SARGON NON-EXPANDABLE DENTAL IMPLANT | DZE Root-Form Endosseous Implant |
| 23 Jun 1999 | K981141 | SARGON IMMEDIATE LOAD IMPLANT, MODEL D | DZE Root-Form Endosseous Implant |
| 8 Jul 1994 | K930071 | SARGON CYLINDRO-BLADE IMPLANT | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: BIODENT INC /Khachi (3).
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.