MedtechSourcebook

Stellartech Research Corp.

Contract manufacturer · Milpitas, CA

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

FDA registration
3010653929 (openFDA record; or search FDA's registration database)
FEI number
3010653929
Registered for
FDA registration year 2026
Establishment types
Manufacturer for export only; Contract manufacturer
Owner or operator
STELLARTECH RESEARCH CORP. (FDA owner/operator no. 9022137)
Registered address
560 Cottonwood Dr, Milpitas, CA 95035
Contract listings
10 device listings, 9 product codes, first listed Feb 1, 2013
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 manufacturingFeb 1, 2013
GXDGenerator, Lesion, RadiofrequencyClass IINeurologyContract manufacturingFeb 1, 2013
JADSystem, Therapeutic, X-RayClass IIRadiologyContract manufacturingFeb 1, 2013
LPBCardiac Ablation Percutaneous CatheterClass IIICardiovascularContract manufacturingJul 30, 2014
OADCatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FlutterClass IIICardiovascularContract manufacturingJul 30, 2014
OAECatheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial FibrillationClass IIICardiovascularContract manufacturingMar 10, 2021
OCMSurgical Cardiac Ablation Device, For Treatment Of Atrial FibrillationClass IIICardiovascularContract manufacturingFeb 1, 2013
OOYBronchial Thermoplasty SystemClass IIIAnesthesiologyContract manufacturingFeb 1, 2013
QYIAblation Catheter, Renal DenervationClass IIICardiovascularContract manufacturingNov 20, 2023