# Entech, Inc.

- Location (FDA's records): Lebanon, NJ
- FDA decisions: 7 (1986–1989): 7 510(k) clearances
- Product codes: KNT (6), FRN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K891371: Gilsdorf Percu. Endo.-Peg & Percu. Flouro.-PFG (Aug 3, 1989)
- K890430: Entainer (TM) Enteral Feeding Container (Jun 2, 1989)
- K873343: Entube-Meer and Meer Feeding Tube Bridle System (Dec 7, 1987)
- K873444: Entech Enteral Pump and Set (Nov 2, 1987)
- K871019: Enfuse Enternal Administration Set & Pump Set (Jun 9, 1987)
- K861427: Entube TM, Enteral Feeding Tube (Jul 18, 1986)
- K861552: Top-Port Enteral Feeding Bag and Preattached Sets (Jun 16, 1986)

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