MedtechSourcebook

TIDI PRODUCTS, LLC

Contract manufacturer ยท Neenah, WI

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

1992Product codes first listed, by year (tallest: 2)2026
FDA registration
2182318 (openFDA record; or search FDA's registration database)
FEI number
2182318
Registered for
FDA registration year 2026
Establishment types
Specification developer; Manufacturer; Contract manufacturer; Repackager or relabeler
Owner or operator
TIDI PRODUCTS, LLC (FDA owner/operator no. 9921057)
Registered address
570 Enterprise Dr, Neenah, WI 54956
Contract listings
13 device listings, 11 product codes, first listed Jul 16, 1992
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
CCWLaryngoscope, RigidClass IAnesthesiologyContract manufacturingApr 30, 2019
EGZHolder, Film, X-RayClass IDentalContract manufacturingJun 12, 2008
EIAUnit, Operative DentalClass IDentalContract manufacturingSep 2, 2022
EYJHolder, Ureteral CatheterClass IGastroenterology and urologyContract manufacturingFeb 8, 2017
GEIElectrosurgical, Cutting & Coagulation & AccessoriesClass IIGeneral and plastic surgeryContract manufacturingMay 3, 2021
IYOSystem, Imaging, Pulsed Echo, UltrasonicClass IIRadiologyContract manufacturingFeb 9, 2022
JEQToothbrush, PoweredClass IDentalContract manufacturingJan 4, 2021
KMKDevice, Intravascular Catheter SecurementClass IGeneral hospitalContract manufacturingOct 27, 2014
KQMCamera, Surgical And AccessoriesClass IGeneral and plastic surgeryContract manufacturingJul 16, 1992
PEMDental Barriers And SleevesClass IIGeneral and plastic surgeryContract manufacturingFeb 20, 2014
QAIPowered Microneedle DeviceClass IIGeneral and plastic surgeryContract manufacturingMar 4, 2025