# KINETEC USA

FEI: 3010675856
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: Kinetec USA, Inc. (#10045573)

Address: N174W21475 Alcan Drive, Jackson, WI, US



## Products

Total registered: 1
Top product codes: ILO
Regulation §: 890.5720


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223010675856%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3010675856