# Owen Mumford USA, Inc.

- Location (FDA's records): Marietta, GA
- FDA decisions: 10 (1995–2001): 10 510(k) clearances
- Product codes: KZH (4), LKY (2), FMF (2), KXP (1), FMI (1)
- Predicates its devices cite: 4 (2 its own); citations of its devices by later devices: 19 (2 its own)
- Recalls linked to its devices: 4 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Ulster Scientific, Inc.: 1 (https://510kreport.com/company/ulster-scientific)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)

## Firms that cite its devices most
- Scandinavian Health Limited: 4 (https://510kreport.com/company/scandinavian-health)
- Owen Mumford, Ltd.: 2 (https://510kreport.com/company/owen-mumford)
- Union Medico Aps: 2 (https://510kreport.com/company/union-medico)
- Innoject, Inc.: 2 (https://510kreport.com/company/innoject)
- Eli Lilly and Company: 1 (https://510kreport.com/company/eli-lilly)
- Biogen: 1 (https://510kreport.com/company/biogen)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)
- Medtronic Minimed: 1 (https://510kreport.com/company/medtronic-minimed)

## Its most-cited devices
- K013362: Autoject 2 (2001), cited by 6
- K945660: Autoject 2 (1995), cited by 5
- K983974: Owen Mumford 3ML Autopen (1998), cited by 2
- K973899: Unifine Pentips (1997), cited by 2
- K983045: Amielle (1998), cited by 1
- K953735: Autoject Mini (1995), cited by 1

## Recent decisions
- K013362: Autoject 2 (Nov 13, 2001)
- K993385: Autojet 2 (Non-Fixed Needle Type) (Nov 10, 1999)
- K983994: Unifine (Jan 8, 1999)
- K983974: Owen Mumford 3ML Autopen (Dec 21, 1998)
- K982275: Rapport V.T.D. (Dec 4, 1998)
- K983045: Amielle (Nov 25, 1998)
- K973899: Unifine Pentips (Dec 4, 1997)
- K971443: Rapport V.T.D. (Sep 26, 1997)

Source page: https://510kreport.com/company/owen-mumford-usa