Not currently registered with FDA under this name
Innova Corp.
Washington, DC, United States. Named as applicant on 5 dental 510(k) clearances between 1995 and 2004. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 51995–2004
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Innova Corp. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 9 Apr 2004 | K040714 | HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT | DZE Root-Form Endosseous Implant |
| 10 Feb 1999 | K984117 | INNOVA TELESCOPIC DISTRACTOR | MQN External Mandibular Fixator and/or Distractor |
| 8 May 1997 | K971196 | ENDOPORE ENDOSSEOUS DENTAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
| 19 Jul 1995 | K952434 | ENDOPORE DENTAL IMPLANT ABUTMENTS | DZE Root-Form Endosseous Implant |
| 13 Feb 1995 | K926354 | ENDO-PORE ENDOSSEOUS DENTAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
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.