MedtechSourcebook

Pentair Filtration Solutions

Contract manufacturer · Saint Paul, MN

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

FDA registration
2132517 (openFDA record; or search FDA's registration database)
FEI number
1000221012
Registered for
FDA registration year 2026
Establishment types
Manufacturer; Contract manufacturer
Owner or operator
Pentair Filtration Solutions (FDA owner/operator no. 9009435)
Registered address
1350 Hammond Rd, Saint Paul, MN 55110
Contract listings
1 device listings, 1 product codes, first listed Mar 4, 2016
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
CAHFilter, Bacterial, Breathing-CircuitClass IIAnesthesiologyContract manufacturingMar 4, 2016