# Inogen, Inc

FEI: 3009843463
Status: Active
Establishment types: Remanufacture Medical Device; Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: INOGEN, INC. (#9064201)

Address: 600 Shiloh Rd., Plano, TX, US



## Products

Total registered: 1
Top product codes: SDT
Regulation §: 868.5665

Proprietary names: SIMEOX 200 Airway Clearance Device

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223009843463%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3009843463