MedtechSourcebook

ASCENTRON, INC.

Contract manufacturer · White City, OR

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

FDA registration
3013069546 (openFDA record; or search FDA's registration database)
FEI number
3013069546
Registered for
FDA registration year 2026
Establishment types
Contract manufacturer
Owner or operator
Ascentron, Inc. (FDA owner/operator no. 10060122)
Registered address
994 Antelope Rd., White City, OR 97503
Contract listings
6 device listings, 9 product codes, first listed Apr 1, 2019
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
GEIElectrosurgical, Cutting & Coagulation & AccessoriesClass IIGeneral and plastic surgeryContract manufacturingNov 15, 2019
GXYElectrode, CutaneousClass IINeurologyContract manufacturingNov 20, 2019
GZJStimulator, Nerve, Transcutaneous, For Pain ReliefClass IINeurologyContract manufacturingApr 1, 2019
ILOPack, Hot Or Cold, Water CirculatingClass IIPhysical medicineContract manufacturingNov 20, 2019
ILYLamp, Infrared, Therapeutic HeatingClass IIPhysical medicineContract manufacturingApr 1, 2019
IMIUltrasonic Diathermy For Use In Applying Therapeutic Deep HeatClass IIPhysical medicineContract manufacturingApr 1, 2019
IPFStimulator, Muscle, PoweredClass IIPhysical medicineContract manufacturingApr 1, 2019
LIHInterferential Current TherapyClass IINeurologyContract manufacturingApr 1, 2019
QZOWearable Vibration Device For Orthopedic UseClass IIOrthopedicContract manufacturingJun 23, 2025