# K102752: Stingray Ultralite Disposable Irrigating Bipolar Forceps

- Pathway: 510(k) (Traditional)
- Applicant: Stingray Surgical Products, Inc.
- Decided: Nov 9, 2011 after 412 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: 6 generations back to K923332 (1992). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K080187: Olsen Medical Single Use Bayonet Bipolar Irrigating Forceps, Olsen Medical (2008) Summary page 1.
- K083162: Stingray Electrosurgical Forceps, Stingray Surgical Products, Inc. (2009) Summary page 1.

## Indications for use
Designed to grasp, manipulate and coagulate selected tissue for single use in general surgical procedures. These forceps can be sold with or without irrigation and are provided sterile. They are connected through a suitable bipolar cable with the bipolar output of an electrosurgical generator and irrigation module. Stingray Ultralite Disposable Irrigation Forceps can be used with bipolar coagulation current. Coagulation is achieved using electrosurgical energy generated by the electro surgical generator unit and activated by a footswitch. The Stingray Ultralite Disposable Irrigation Forceps have not been shown to be effective for tubal sterilization or tubal coagulation for sterilization procedures and should not be used for these procedures.

Source page: https://510kreport.com/device/K102752
Methodology: https://510kreport.com/methodology