MedtechSourcebook

Crosstex International

Contract manufacturer ยท Rush, NY

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

1988Product codes first listed, by year (tallest: 1)2026
FDA registration
1319130 (openFDA record; or search FDA's registration database)
FEI number
1319130
Registered for
FDA registration year 2026
Establishment types
Specification developer; Manufacturer; Contract manufacturer; Repackager or relabeler
Owner or operator
SPS/Crosstex International (FDA owner/operator no. 1319130)
Registered address
6789 WEST HENRIETTA RD., Rush, NY 14543
Contract listings
5 device listings, 2 product codes, first listed Jul 11, 1988
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.

Product codeDevice (FDA name)ClassCategoryRoleFirst listed
JOJIndicator, Physical/Chemical Sterilization ProcessClass IIGeneral hospitalContract manufacturingNov 27, 2007
JRGBlock, HeatingClass IClinical chemistryContract manufacturingJul 11, 1988