# CENTRIX, INC.

FEI: 1281412
Status: Active
Establishment types: Repack or Relabel Medical Device; Develop Specifications But Do Not Manufacture At This Facility
Owner/operator: Centrix, Inc. (#1281412)

Address: 770 River Rd, Shelton, CT, US



## Products

Total registered: 2
Top product codes: MVL, ELW
Regulation §: 872.3660


## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221281412%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1281412