# Path Medical GmbH

- Location (FDA's records): Germering, DE
- FDA decisions: 6 (2010–2022): 6 510(k) clearances
- Product codes: GWJ (4), EWO (2)
- Predicates its devices cite: 10 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Gn Otometrics: 2 (https://510kreport.com/company/gn-otometrics)
- Fischer-Zoth Audiologic Systems, Inc.: 2 (https://510kreport.com/company/fischer-zoth-audiologic-systems)
- Bio-Logic Systems Corp.: 1 (https://510kreport.com/company/bio-logic-systems)
- Interacoustics AS: 1 (https://510kreport.com/company/interacoustics)
- Interacoustics A/S: 1 (https://510kreport.com/company/interacoustics-a-s)
- Natus Medical, Inc.: 1 (https://510kreport.com/company/natus-medical)

## Firms that cite its devices most
- Db Diagnostic Systems, Inc.: 1 (https://510kreport.com/company/db-diagnostic-systems)

## Its most-cited devices
- K133012: Sentiero (2014), cited by 3

## Recent decisions
- K220139: QScreen (Aug 3, 2022)
- K213345: Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONE (Jun 22, 2022)
- K211147: ALGO 7i (Oct 14, 2021)
- K133012: Sentiero (Jun 9, 2014)
- K131141: Earprobe (Jun 27, 2013)
- K100661: Earprobe (Jul 1, 2010)

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