# Scopis GmbH

- Location (FDA's records): Berlin, DE
- FDA decisions: 2 (2017–2017): 2 510(k) clearances
- Product codes: PGW (2)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 5 (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
- Fiagon GmbH: 2 (https://510kreport.com/company/fiagon)
- Brainlab AG: 1 (https://510kreport.com/company/brainlab)

## Firms that cite its devices most
- Stryker Ent: 3 (https://510kreport.com/company/stryker-ent)
- Stryker Corp.: 2 (https://510kreport.com/company/stryker)

## Its most-cited devices
- K161491: Scopis Hybrid Navigation System EM (2017), cited by 3
- K171661: Scopis Extended Instrument Set EM (2017), cited by 2

## Recent decisions
- K171661: Scopis Extended Instrument Set EM (Sep 27, 2017)
- K161491: Scopis Hybrid Navigation System EM (Feb 9, 2017)

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