FDA Device Establishments · JSON-LD · Markdown

Starkey Global Distribution Center

FEI 3019622583 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active

FEI Number3019622583
Owner / OperatorStarkey Laboratories, Inc. (#2125608)
Address3810 Plainfield Road, Suite#112, Plainfield, IN, US
Registration expiry2026
Initial importer flagY
Registered products1
Product codes (top 20)ESD
Regulation § (21 CFR)874.3300
Proprietary namesStarkey X Series; MicroTech Propel; Audibel A4 iQ; NuEar Signature Series; Amplifon ampli-mini; Audibel Invisibel Synergy; NuEar canvas; Starkey Muse iQ; Starkey Signature Series; NuEar SDS

External sources

Source: openFDA. Public-domain (CC0).