# K213042: Supra Non-Stick Bipolar Forceps

- Pathway: 510(k) (Abbreviated)
- Applicant: Guenter Bissinger Medizintechnik GmbH
- Decided: Nov 17, 2022 after 421 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K923332 (1992). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051429: Claris Non-Stick Bipolar Forceps, Guenter Bissinger Medizintechnik GmbH (2005) Summary page 5.

## Indications for use
The Bissinger SUPRA Non-Stick Bipolar Forceps are used for grasping, dissection and coagulation of biological tissues. The fully assembled instrument (if assembly is needed) has to be connected — with the appropriate cable - to the bipolar output of an HF generator. Supra Non-Stick Bipolar Forceps may not be used for tubal sterilization or tubal coagulation.

Source page: https://510kreport.com/device/K213042
Methodology: https://510kreport.com/methodology