# Stingray Surgical Products, Inc.

- Location (FDA's records): Boca Raton, FL
- FDA decisions: 3 (2009–2013): 3 510(k) clearances
- Names in FDA's records: Stingray Surgical Products, Inc. (2); Stingray Surgical Products (1)
- Product codes: GEI (3)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Pro Med Instruments GmbH: 1 (https://510kreport.com/company/pro-med-instruments)
- Olsen Medical: 1 (https://510kreport.com/company/olsen-medical)

## Firms that cite its devices most
- Stryker Leibinger GmbH & Co KG: 1 (https://510kreport.com/company/stryker-leibinger)

## Its most-cited devices
- K083162: Stingray Electrosurgical Forceps (2009), cited by 3

## Recent decisions
- K123478: Stingray Bipolar Forceps (May 10, 2013)
- K102752: Stingray Ultralite Disposable Irrigating Bipolar Forceps (Nov 9, 2011)
- K083162: Stingray Electrosurgical Forceps (Jan 12, 2009)

Source page: https://510kreport.com/company/stingray-surgical-products