# OWEN MUMFORD USA, INC.

FEI: 1000219614
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Repack or Relabel Medical Device
Owner/operator: OWEN MUMFORD, LTD. (#8021764)

Address: 1755 W Oak Commons Ct, MARIETTA, GA, US



## Products

Total registered: 1
Top product codes: KZH
Regulation §: 880.6920

Proprietary names: AUTOJECT 2 (NON-FIXED NEEDLE), Betaject Lite, Extavia Auto-Injector II

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221000219614%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1000219614