FDA Device Establishments · JSON-LD · Markdown

OWEN MUMFORD USA, INC.

FEI 1000219614 · Complaint File Establishment per 21 CFR 820.198 Repack or Relabel Medical Device · Status: Active

FEI Number1000219614
Owner / OperatorOWEN MUMFORD, LTD. (#8021764)
Address1755 W Oak Commons Ct, MARIETTA, GA, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)KZH
Regulation § (21 CFR)880.6920
Proprietary namesAUTOJECT 2 (NON-FIXED NEEDLE); Betaject Lite; Extavia Auto-Injector II

External sources

Source: openFDA. Public-domain (CC0).