# Endo-Therapeutics, Inc.

- Location (FDA's records): Safety Harbor, FL
- FDA decisions: 7 (1993–2009): 7 510(k) clearances
- Product codes: FBK (1), FCL (1), KNS (1), KGE (1), OCY (1), DRF (1), GEI (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Boston Scientific Corp: 1 (https://510kreport.com/company/boston-scientific)
- Flexmedics: 1 (https://510kreport.com/company/flexmedics)
- Radius Medical Technologies, Inc.: 1 (https://510kreport.com/company/radius-medical-technologies)

## Firms that cite its devices most
- Zutron Medical, LLC: 1 (https://510kreport.com/company/zutron-medical)

## Its most-cited devices
- K023603: Endo-Glide Guidewire (2003), cited by 1

## Recent decisions
- K090796: Multi-Bite Hot Biopsy Forceps (Nov 25, 2009)
- K031026: Eti Bipolar Hemostatic Probe (Jun 27, 2003)
- K023603: Endo-Glide Guidewire (Feb 19, 2003)
- K012725: Tissue Grasping Forceps, Scissors, Clamps and Dissectors for Laparoscopic Surgeries (Nov 8, 2001)
- K012977: Varices Injection Needle (Nov 2, 2001)
- K926549: Endocath Electrophysiology Catheter (Dec 6, 1993)
- K925392: Biopsy Forceps (Nov 5, 1993)

Source page: https://510kreport.com/company/endo-therapeutics