MedtechSourcebook

AXCESOR LLC

Contract manufacturer ยท Menomonee Falls, WI

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

2012Product codes first listed, by year (tallest: 3)2026
FDA registration
2134752 (openFDA record; or search FDA's registration database)
FEI number
3003007822
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
AXCESOR LLC (FDA owner/operator no. 9012066)
Registered address
W134N5345 Campbell Drive, Menomonee Falls, WI 53051
Contract listings
10 device listings, 8 product codes, first listed Dec 26, 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
BTAPump, Portable, Aspiration (Manual Or Powered)Class IIGeneral and plastic surgeryContract manufacturingJul 17, 2024
BTLVentilator, Emergency, Powered (Resuscitator)Class IIAnesthesiologyContract manufacturingDec 26, 2012
CAPMonitor, Airway Pressure (Includes Gauge And/Or Alarm)Class IIAnesthesiologyContract manufacturingDec 3, 2018
CCKAnalyzer, Gas, Carbon-Dioxide, Gaseous-PhaseClass IIAnesthesiologyContract manufacturingDec 26, 2012
DQAOximeterClass IICardiovascularContract manufacturingDec 26, 2012
DSACable, Transducer And Electrode, Patient, (Including Connector)Class IICardiovascularContract manufacturingDec 2, 2022
EMFKnife, SurgicalClass IGeneral and plastic surgeryContract manufacturingJan 8, 2025
HRXArthroscopeClass IIOrthopedicContract manufacturingJan 8, 2025