# Kentec Medical, Inc.

- Location (FDA's records): Irvine, CA
- FDA decisions: 6 (1985–2012): 6 510(k) clearances
- Product codes: FMT (2), KNT (1), DRX (1), FRW (1), FPD (1)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 9 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Neomed, Inc.: 3 (https://510kreport.com/company/neomed)
- Corpak Medsystems: 2 (https://510kreport.com/company/corpak-medsystems)
- Neotech Products, Inc.: 1 (https://510kreport.com/company/neotech-products)

## Firms that cite its devices most
- Vr Medical Technology Co., Ltd.: 2 (https://510kreport.com/company/vr-medical-technology)
- R & D Medical Products, Inc.: 1 (https://510kreport.com/company/r-d-medical-products)
- Replacement Parts Industries, Inc.: 1 (https://510kreport.com/company/replacement-parts-industries)

## Its most-cited devices
- K120272: Ameritus Medical Enteral Feeding Extension Set (2012), cited by 1
- K970686: Accutemp-Probe (1997), cited by 1
- K050443: Accu-Lead (2005), cited by 1
- K100526: Ameritus Entral (TM) Enteral Feeding Tube (2010), cited by 1

## Recent decisions
- K120272: Ameritus Medical Enteral Feeding Extension Set (Feb 17, 2012)
- K100526: Ameritus Entral (TM) Enteral Feeding Tube (Apr 22, 2010)
- K050443: Accu-Lead (Sep 2, 2005)
- K970686: Accutemp-Probe (Aug 25, 1997)
- K960080: Accutemp Probe (May 1, 1996)
- K853475: Gram-MA Neonatal SC (Sep 5, 1985)

Source page: https://510kreport.com/company/kentec-medical