# Exel Intl.

- Location (FDA's records): Culver City, CA
- FDA decisions: 18 (1986–2000): 18 510(k) clearances
- Product codes: FPA (6), FMI (4), FIE (1), FDZ (1), FOZ (1), FMK (1), FMG (1), GIM (1), DZM (1), FMF (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 10 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Nipro Medical Corporation: 6 (https://510kreport.com/company/nipro-medical)
- Bioteque Corp.: 1 (https://510kreport.com/company/bioteque)
- Cytori Therapeutics, Inc.: 1 (https://510kreport.com/company/cytori-therapeutics)
- Nissho Corp.: 1 (https://510kreport.com/company/nissho)
- Busse Hospital Disposables, Inc.: 1 (https://510kreport.com/company/busse-hospital-disposables)

## Its most-cited devices
- K895769: Exel Huber Needle (1990), cited by 2
- K861152: Exel Vacuum Blood Collecting System (1986), cited by 2
- K895770: Exel Huber Infusion Set (1990), cited by 2
- K895771: Exel Spinal Needles (1990), cited by 1
- K895768: Exel Safelet Catheter (1990), cited by 1
- K862491: Exel Butterfly Scalp Vein Set (1986), cited by 1

## Recent decisions
- K992290: Exel Injection Plug with Cap (Feb 23, 2000)
- K963658: Exel Avf Single Needle (May 5, 1998)
- K963659: Exel I.V. Administration Set (Dec 16, 1997)
- K926119: Exel Huber Infusion Set Rotating Wing (Aug 11, 1993)
- K904685: Exel Huber Infusion Set Without Injection Site (Y) (Nov 21, 1990)
- K903945: Exel a-V Fistula Set (Nov 20, 1990)
- K895770: Exel Huber Infusion Set (Jul 19, 1990)
- K895769: Exel Huber Needle (Feb 16, 1990)

Source page: https://510kreport.com/company/exel-intl