# Trokamed GmbH

- Location (FDA's records): Geisingen, DE
- FDA decisions: 4 (2006–2021): 4 510(k) clearances
- Product codes: FED (1), GCJ (1), GEI (1), HET (1)
- Predicates its devices cite: 14 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 15 (4 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Richard Wolf Medical Instruments Corp.: 4 (https://510kreport.com/company/richard-wolf-medical-instruments)
- KARL STORZ Endoscopy-America, Inc.: 2 (https://510kreport.com/company/karl-storz-endoscopy-america)
- Hans Hermann GmbH: 1 (https://510kreport.com/company/hans-hermann)
- Ackermann Instrumente GmbH: 1 (https://510kreport.com/company/ackermann-instrumente)
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)
- Megadyne Medical Products, Inc.: 1 (https://510kreport.com/company/megadyne-medical-products)
- Guenter Bissinger Medizintechnik GmbH: 1 (https://510kreport.com/company/guenter-bissinger-medizintechnik)
- Comeg Endoscopy: 1 (https://510kreport.com/company/comeg-endoscopy)

## Firms that cite its devices most
- Gimmi GmbH: 1 (https://510kreport.com/company/gimmi)

## Its most-cited devices
- K060232: Trokamed GMBH Electrosurgical Instruments & Accessories (2006), cited by 1

## Recent decisions
- K200770: Mini PCNL-System (Jul 30, 2021)
- K091010: Trokamed Morcellator (Mar 1, 2011)
- K060233: Trokamed GMBH Endoscopes and Accessories (Jul 19, 2006)
- K060232: Trokamed GMBH Electrosurgical Instruments & Accessories (Jul 12, 2006)

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