MedtechSourcebook

TRICOR SYSTEMS

Contract manufacturer ยท Elgin, IL

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

2007Product codes first listed, by year (tallest: 3)2026
FDA registration
1423929 (openFDA record; or search FDA's registration database)
FEI number
3001451660
Registered for
FDA registration year 2027
Establishment types
Manufacturer; Contract manufacturer
Owner or operator
TRICOR SYSTEMS (FDA owner/operator no. 9032214)
Registered address
1650 TODD FARM DR., Elgin, IL 60123
Contract listings
8 device listings, 7 product codes, first listed Oct 24, 2007
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
EJISyringe, CartridgeClass IIDentalContract manufacturingOct 24, 2007
FCYBulb, Inflation, For EndoscopeClass IGastroenterology and urologyContract manufacturingNov 2, 2007
FMFSyringe, PistonClass IIGeneral hospitalContract manufacturingJun 21, 2018
IYTSystem, Rebreathing, RadionuclideClass IIRadiologyContract manufacturingFeb 21, 2020
IZDProbe, Uptake, NuclearClass IRadiologyContract manufacturingDec 22, 2020
KDNSystem, Perfusion, KidneyClass IIGastroenterology and urologyContract manufacturingDec 4, 2013
PSWHigh Level Disinfection Reprocessing Instrument For Ultrasonic Transducers, LiquidClass IIRadiologyContract manufacturingNov 2, 2007