# Nipro Diabetes Systems, Inc.

- Location (FDA's records): Lexington, KY
- FDA decisions: 5 (2001–2007): 5 510(k) clearances
- Product codes: LZG (3), FMF (1), FPA (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 3 (2 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Disetronic Medical Systems: 1 (https://510kreport.com/company/disetronic-medical-systems)
- Medtronic Minimed: 1 (https://510kreport.com/company/medtronic-minimed)
- Animas Corp.: 1 (https://510kreport.com/company/animas)
- Smiths Medical MD, Inc.: 1 (https://510kreport.com/company/smiths-medical-md)

## Firms that cite its devices most
- Tandem Diabetes Care, Inc.: 1 (https://510kreport.com/company/tandem-diabetes-care)

## Its most-cited devices
- K013309: Glucopro Evo Infusion Pump (2002), cited by 1
- K050312: Amigo Insulin Pump (2005), cited by 1
- K071613: Amigo Insulin Pump (2007), cited by 1

## Recent decisions
- K071613: Amigo Insulin Pump (Dec 14, 2007)
- K050312: Amigo Insulin Pump (May 9, 2005)
- K014114: Glucopro Syringe, Model Gpsy-Xxxxxxxx (Jun 26, 2002)
- K013309: Glucopro Evo Infusion Pump (Jun 24, 2002)
- K011120: Glucopro Infusion Set, Model Gpisxxxxxxxx Series (May 8, 2001)

Source page: https://510kreport.com/company/nipro-diabetes-systems