# MYKITA NORTH AMERICA

FEI: 3005516815
Status: Active
Establishment types: Repack or Relabel Medical Device
Owner/operator: MYKITA North America (#10044968)

Address: 80 Main St Ste 200, West Orange, NJ, US



## Products

Total registered: 1
Top product codes: HQZ
Regulation §: 886.5842

Proprietary names: MYKITA MYLON, MYKITA, MYKITA Lite, MYKITA Col No.1, MYKITA Col No.2

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005516815%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005516815