# Bema-GmbH & Co. KG

- Location (FDA's records): Amsterdam, NL
- FDA decisions: 1 (2011–2011): 1 510(k) clearance
- Product codes: GEI (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Antyllos Medizintechnik GmbH: 1 (https://510kreport.com/company/antyllos-medizintechnik)
- Pajunk GmbH: 1 (https://510kreport.com/company/pajunk)
- Aesculap, Inc.: 1 (https://510kreport.com/company/aesculap)
- Tekno Medical Optik-Chirurgie GmbH & Co.: 1 (https://510kreport.com/company/tekno-medical-optik-chirurgie)

## Firms that cite its devices most
- Hunan Handlike Minimally Invasive Surgery Co., Ltd.: 1 (https://510kreport.com/company/hunan-handlike-minimally-invasive-surgery)
- Carefusion 2200, Inc.: 1 (https://510kreport.com/company/carefusion-2200)

## Its most-cited devices
- K102921: Endoscopic Monopolar Instruments and Accessories (2011), cited by 2

## Recent decisions
- K102921: Endoscopic Monopolar Instruments and Accessories (Dec 20, 2011)

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