# Het Systems, LLC

- Location (FDA's records): Iselin, NJ
- FDA decisions: 3 (2011–2014): 3 510(k) clearances
- Product codes: GEI (3)
- Predicates its devices cite: 8 (2 its own); citations of its devices by later devices: 3 (2 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
- Valleylab, Inc.: 1 (https://510kreport.com/company/valleylab)
- Silverglide Surgical Technologies: 1 (https://510kreport.com/company/silverglide-surgical-technologies)
- Stryker Leibinger GmbH & Co KG: 1 (https://510kreport.com/company/stryker-leibinger)
- Guenter Bissinger Medizintechnik GmbH: 1 (https://510kreport.com/company/guenter-bissinger-medizintechnik)
- Curon Medical, Inc.: 1 (https://510kreport.com/company/curon-medical)
- Hogan & Hartson: 1 (https://510kreport.com/company/hogan-hartson)

## Firms that cite its devices most
- Covidien: 1 (https://510kreport.com/company/covidien)

## Its most-cited devices
- K140422: Het Systems, LLC, Het Bipolar Ligator System (2014), cited by 1
- K110143: Het Bipolar Electrocautery Forceps (2011), cited by 1
- K121085: Het Bipolar Ligator System (2012), cited by 1

## Recent decisions
- K140422: Het Systems, LLC, Het Bipolar Ligator System (Jun 5, 2014)
- K121085: Het Bipolar Ligator System (Nov 20, 2012)
- K110143: Het Bipolar Electrocautery Forceps (Jun 2, 2011)

Source page: https://510kreport.com/company/het-systems