# Pausch Medical GmbH

- Location (FDA's records): Erlangen, DE
- FDA decisions: 3 (2016–2023): 3 510(k) clearances
- Product codes: JAA (2), IZF (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Agfa Corp.: 1 (https://510kreport.com/company/agfa)
- Orthoscan, Inc.: 1 (https://510kreport.com/company/orthoscan)
- Siemens Medical Solutions USA, Inc.: 1 (https://510kreport.com/company/siemens-medical-solutions-usa)

## Firms that cite its devices most
- Adaptix Limited: 1 (https://510kreport.com/company/adaptix)
- KARL STORZ Endoscopy-America, Inc.: 1 (https://510kreport.com/company/karl-storz-endoscopy-america)

## Its most-cited devices
- K161019: Uroview FD (2016), cited by 2
- K221949: Ortho Device, ADAPTIX 3D Orthopedic Imaging System (2023), cited by 1

## Recent decisions
- K221949: Ortho Device, ADAPTIX 3D Orthopedic Imaging System (Jan 26, 2023)
- K180651: Uroview FD II (Apr 12, 2018)
- K161019: Uroview FD (Aug 17, 2016)

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