# Lanterna Medical Technologies

- Location (FDA's records): St.Gallen, CH
- FDA decisions: 2 (2014–2015): 2 510(k) clearances
- Product codes: NKB (2)
- Predicates its devices cite: 2 (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
- GS Medical Co., Ltd.: 1 (https://510kreport.com/company/gs-medical)

## Firms that cite its devices most
- Grafton Medical Alliance: 1 (https://510kreport.com/company/grafton-medical-alliance)

## Its most-cited devices
- K133063: Santis Pedicle Screw System (2014), cited by 2

## Recent decisions
- K150507: Santis Pedicle Screw System (Apr 3, 2015)
- K133063: Santis Pedicle Screw System (Jan 13, 2014)

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