Not currently registered with FDA under this name
Dio Department Dsi, Inc.
Los Angeles, CA, United States. Named as applicant on 8 dental 510(k) clearances between 2006 and 2008. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 82006–2008
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2000–2026
510(k) clearances
Clearances on which FDA names Dio Department Dsi, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 30 May 2008 | K080129 | SECURE IMPLANT SYSTEM (2.5/3.0MM) | DZE Root-Form Endosseous Implant |
| 16 May 2008 | K073070 | DIO BIOTITE-H IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 14 May 2008 | K080128 | SM-EXTRA WIDE (RBM) IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 15 Apr 2008 | K070570 | DIO IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 11 Apr 2008 | K080126 | DIO PROTEM IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 8 Nov 2007 | K070569 | SM INTERNAL./EXTERNAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 25 May 2007 | K070568 | DIO PROTEM IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 1 Sep 2006 | K061797 | SM IMPLANT SYSTEMS | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: DIO Corporation (7).
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.