# Hans Hermann GmbH

- Location (FDA's records): Wurmlingen, DE
- FDA decisions: 2 (1998–2005): 2 510(k) clearances
- Product codes: GCJ (1), JEY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Trokamed GmbH: 1 (https://510kreport.com/company/trokamed)
- Elmed, Inc.: 1 (https://510kreport.com/company/elmed)
- Vibrynt, Inc.: 1 (https://510kreport.com/company/vibrynt)
- Guenter Bissinger Medizintechnik GmbH: 1 (https://510kreport.com/company/guenter-bissinger-medizintechnik)

## Its most-cited devices
- K051610: Hans Hermann Laparoscopes and Accessories (2005), cited by 4

## Recent decisions
- K051610: Hans Hermann Laparoscopes and Accessories (Jul 29, 2005)
- K983535: The Titanium Miniplating System, the Titanium Microplating System, the Titanium Mediumplating System, Model #'S H12-1010 (Dec 29, 1998)

Source page: https://510kreport.com/company/hans-hermann