MedtechSourcebook

PLEXUS CORP.

Contract manufacturer · Neenah, WI

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

FDA registration
2183715 (openFDA record; or search FDA's registration database)
FEI number
2183715
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
PLEXUS CORP. (FDA owner/operator no. 3019588)
Registered address
2444 Schultz Drive, Neenah, WI 54956
Contract listings
6 device listings, 7 product codes, first listed Jan 15, 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
DQKComputer, Diagnostic, ProgrammableClass IICardiovascularContract manufacturingJan 15, 2016
GEIElectrosurgical, Cutting & Coagulation & AccessoriesClass IIGeneral and plastic surgeryContract manufacturingNov 28, 2018
HGIElectrocautery, Gynecologic (And Accessories)Class IIObstetrics and gynecologyContract manufacturingFeb 26, 2025
LFLInstrument, Ultrasonic SurgicalUnclassifiedGeneral and plastic surgeryContract manufacturingFeb 26, 2025
MRZAccessories, Pump, InfusionClass IIGeneral hospitalContract manufacturingSep 11, 2017
NSUInstrumentation For Clinical Multiplex Test SystemsClass IIClinical chemistryContract manufacturingFeb 10, 2022
SIRIntegrated Operating Table-Electromechanical Surgical SystemClass IIGeneral and plastic surgeryContract manufacturingAug 20, 2026

Other contract facilities of PLEXUS CORP.