# Promimic AB

- Location (FDA's records): Goteborg, SE
- FDA decisions: 2 (2011–2026): 2 510(k) clearances
- Product codes: DZE (2)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Implant Direct, LLC: 1 (https://510kreport.com/company/implant-direct)
- Implant Innovations, Inc.: 1 (https://510kreport.com/company/implant-innovations)
- Nobelpharma USA, Inc.: 1 (https://510kreport.com/company/nobelpharma-usa)
- Astra Tech, Inc.: 1 (https://510kreport.com/company/astra-tech)

## Firms that cite its devices most
- S.I.N. - Sistema DE Implante Nacional S.A.: 1 (https://510kreport.com/company/sin-sistema-de-implante-nacional)

## Its most-cited devices
- 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 (2011), cited by 2

## Recent decisions
- K252731: Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental Implant (May 12, 2026)
- 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 (Jan 25, 2011)

Source page: https://510kreport.com/company/promimic