# Flexible Stenting Solutions, Inc.

- Location (FDA's records): Eatontown, NJ
- FDA decisions: 5 (2009–2012): 5 510(k) clearances
- Product codes: FGE (5)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 9 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K121125: Flexstent Biliary Self-Expanding Stent System (Jul 6, 2012)
- K120452: Flexstent Biliary Self-Expanding Stent System (Apr 24, 2012)
- K112522: Flexstent Biliary Self-Expanding Stent System (Dec 30, 2011)
- K102519: Flexstent Biliary Self Expanding Stent System Model FLX-Ddlll-BX (Nov 22, 2010)
- K081996: Flexstent Biliary Self Expanding Stent System (Sep 15, 2009)

Source page: https://510kreport.com/company/flexible-stenting-solutions