# Gunter Bissinger Medizintechnik GmbH

- Location (FDA's records): Teningen, DE
- FDA decisions: 2 (2004–2018): 2 510(k) clearances
- Product codes: GEI (1), HET (1)
- Predicates its devices cite: 2 (0 its own); citations of its devices by later devices: 3 (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
- Sutter Medizintechnik GmbH: 1 (https://510kreport.com/company/sutter-medizintechnik)
- Guenter Bissinger Medizintechnik GmbH: 1 (https://510kreport.com/company/guenter-bissinger-medizintechnik)

## Firms that cite its devices most
- Prana Surgical: 1 (https://510kreport.com/company/prana-surgical)
- Jiangsu Hope Biomedical Science & Technology Co., Ltd.: 1 (https://510kreport.com/company/jiangsu-hope-biomedical-science-technology)
- Kl Martin L.P.: 1 (https://510kreport.com/company/kl-martin)

## Its most-cited devices
- K172368: Bipolar Micro-Coagulation Forceps (2018), cited by 2
- K033177: Powergrip Bipolar Coagulation Forceps, Model 824XXXXX (2004), cited by 1

## Recent decisions
- K172368: Bipolar Micro-Coagulation Forceps (Apr 5, 2018)
- K033177: Powergrip Bipolar Coagulation Forceps, Model 824XXXXX (Mar 11, 2004)

Source page: https://510kreport.com/company/gunter-bissinger-medizintechnik
