# Medegen Medical Manufacturing Services

- Location (FDA's records): Ontario, CA
- FDA decisions: 5 (2004–2008): 5 510(k) clearances
- Names in FDA's records: Medegen Medical Manufacturing Services (4); Medegen Medical Manufacturing Services, Inc. (1)
- Product codes: FPA (3), FMG (1), FMF (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 24 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Icu Medical, Inc.: 2 (https://510kreport.com/company/icu-medical)
- The Kipp Group: 1 (https://510kreport.com/company/kipp-group)
- Baxter Healthcare Corp: 1 (https://510kreport.com/company/baxter-healthcare)

## Firms that cite its devices most
- Care Fusion: 3 (https://510kreport.com/company/care-fusion)
- Promepla: 1 (https://510kreport.com/company/promepla)
- One Stick, LLC: 1 (https://510kreport.com/company/one-stick)

## Its most-cited devices
- K051499: Intravascular Administration Set and Extension Set (2005), cited by 5

## Recent decisions
- K083765: Maxguard Advanced Luer Activated Device with Antimicrobial (Dec 30, 2008)
- K052330: Tru-Swab Stocock (Sep 9, 2005)
- K051930: Drug Access Spike (Aug 16, 2005)
- K051499: Intravascular Administration Set and Extension Set (Jun 22, 2005)
- K041179: Modification to the Nac Plus Needleless Access Connector (Jun 4, 2004)

Source page: https://510kreport.com/company/medegen-medical-manufacturing-services