Not currently registered with FDA under this name
Promimic AB
Mölndal, Sweden. Named as applicant on 2 dental 510(k) clearances between 2011 and 2026. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 22011–2026
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Promimic AB as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 12 May 2026 | K252731 | Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental Implant | DZE Root-Form Endosseous Implant |
| 25 Jan 2011 | K101225 | PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 8.5 MM MODEL 03-1001, PROMIMIC DENTAL IMPLANT, 3.75 MM, LENGTH 10 MM MODEL 03-1 | 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.