CENTRIX, INC.

Contract manufacturer · Shelton, CT

FDA-registered (openFDA, export of Oct 21, 2026) ISO 13485: not verified

FDA registration

1281412 (openFDA record; or search FDA's registration database)

FEI number

1281412

Registered for

FDA registration year 2026

Establishment types

Specification developer; Manufacturer; Contract manufacturer; Repackager or relabeler

Owner or operator

Centrix, Inc. (FDA owner/operator no. 1281412)

Registered address

770 River Rd, Shelton, CT 06484

Contract listings

5 device listings, 5 product codes, first listed Aug 10, 1992

Certification

Not verified. We have no certification data for this facility yet.

Devices listed as contract work

Each row is an FDA product code this facility lists under its contract establishment type, with the date of its earliest such listing.