MedtechSourcebook

Trelleborg Sealing Solutions River Falls

Contract manufacturer · River Falls, WI

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

FDA registration
3002939152 (openFDA record; or search FDA's registration database)
FEI number
3002939152
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Trelleborg Sealing Solutions Plymouth LLC (FDA owner/operator no. 9102441)
Registered address
434 Highland Dr, River Falls, WI 54022
Contract listings
2 device listings, 2 product codes, first listed Dec 14, 2012
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
HXSTwister, WireClass IOrthopedicContract manufacturingDec 14, 2012
KJFSystem, Suspension, Cell CultureClass IHematologyContract manufacturingMay 13, 2022

Other contract facilities of Trelleborg Sealing Solutions Plymouth LLC