# Starkey Global Distribution Center

FEI: 3019622583
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: Starkey Laboratories, Inc. (#2125608)

Address: 3810 Plainfield Road, Suite#112, Plainfield, IN, US



## Products

Total registered: 1
Top product codes: ESD
Regulation §: 874.3300

Proprietary names: Starkey 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

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223019622583%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3019622583