# Crospon, Ltd.

- Location (FDA's records): Bonita Springs, FL
- FDA decisions: 12 (2009–2019): 12 510(k) clearances
- Product codes: FFX (7), PIE (2), PID (1), FED (1), KNT (1)
- Predicates its devices cite: 20 (11 its own); citations of its devices by later devices: 14 (11 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- G & J Electronics, Inc.: 3 (https://510kreport.com/company/g-j-electronics)
- Wilson-Cook Medical, Inc.: 1 (https://510kreport.com/company/wilson-cook-medical)
- United States Endoscopy Group, Inc.: 1 (https://510kreport.com/company/united-states-endoscopy-group)
- Smart Medical Systems, Ltd.: 1 (https://510kreport.com/company/smart-medical-systems)
- Bioenterics Corp.: 1 (https://510kreport.com/company/bioenterics)
- Sandhill Scientific, Inc.: 1 (https://510kreport.com/company/sandhill-scientific)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)

## Firms that cite its devices most
- Covidien: 1 (https://510kreport.com/company/covidien)
- C2 Therapeutics, Inc.: 1 (https://510kreport.com/company/c2-therapeutics)
- Boehringer Laboratories: 1 (https://510kreport.com/company/boehringer-laboratories)

## Its most-cited devices
- K092850: Endoflip (2009), cited by 4
- K120997: Barostat Software Option (2012), cited by 3
- K160725: EndoFLIP (2016), cited by 2
- K142000: Esoflip ES (2014), cited by 1
- K110531: Endoflip Ecd (2011), cited by 1
- K110529: Endoflip Gastric Tube (2011), cited by 1

## Recent decisions
- K183072: EndoFLIP System (Feb 15, 2019)
- K172128: EsoFLIP® ES-310 Balloon Catheter (Nov 22, 2017)
- K170833: EndoFLIP® System with FLIP Topography module (Apr 17, 2017)
- K160725: EndoFLIP (May 1, 2016)
- K142000: Esoflip ES (Sep 25, 2014)
- K132337: Esoflip Balloon Dilation Catheter (Oct 7, 2013)
- K130906: Endoflip Catheter (Jul 17, 2013)
- K120997: Barostat Software Option (Aug 27, 2012)

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