# Instent, Inc.

- Location (FDA's records): Eden Prairie, MN
- FDA decisions: 4 (1995–1996): 4 510(k) clearances
- Product codes: FGE (2), ESW (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 4 (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 that cite its devices most
- Medtronic Instent, Inc.: 2 (https://510kreport.com/company/medtronic-instent)
- Medtech Instruments: 2 (https://510kreport.com/company/medtech-instruments)

## Its most-cited devices
- K955041: Instent Esophacoil Self-Expanding Stent System (1996), cited by 2
- K941487: Instent Esophacoil Esophageal Prosthesis (1995), cited by 2

## Recent decisions
- K955041: Instent Esophacoil Self-Expanding Stent System (Feb 21, 1996)
- K945498: Instent Endocoil-T (TM) Transhepatic Biliary Endoprosthesis (Sep 12, 1995)
- K924387: Instent Endocoil Biliary Endoprosthesis (Sep 8, 1995)
- K941487: Instent Esophacoil Esophageal Prosthesis (Feb 23, 1995)

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