# Tellos Medical AB

- Location (FDA's records): Goteborg, SE
- FDA decisions: 1 (2016–2016): 1 510(k) clearance
- Product codes: EKX (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 3 (0 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
- Osstell AB: 1 (https://510kreport.com/company/osstell)

## Firms that cite its devices most
- Hiossen, Inc.: 1 (https://510kreport.com/company/hiossen)
- Dentis Co., Ltd.: 1 (https://510kreport.com/company/dentis)
- Osstell AB: 1 (https://510kreport.com/company/osstell)

## Its most-cited devices
- K143445: Tellos ISQ Buddy (2016), cited by 3

## Recent decisions
- K143445: Tellos ISQ Buddy (Jan 7, 2016)

Source page: https://510kreport.com/company/tellos-medical