BEUDAMED
    FDA Registration Active 🇺🇸 United States

    Stellartech Research Corp.

    Reg #: 3010653929 · FEI: 3010653929 · Expires 2026
    View on FDA
    Products
    10
    Proprietary Names
    7
    Establishment Types
    2
    Classifications
    10

    Registration Details

    Registration Name
    Stellartech Research Corp.
    Registration Number
    3010653929
    FEI Number
    3010653929
    Status
    Active
    Expiry Year
    2026
    Initial Importer
    No
    Address
    560 Cottonwood Dr
    City
    Milpitas
    State
    CA
    ZIP
    95035
    Country
    US

    Owner / Operator

    Firm Name
    STELLARTECH RESEARCH CORP.
    Operator Number
    9022137
    Address
    560 Cottonwood Drive, --
    City
    Milpitas
    State
    CA
    Postal Code
    95035
    Country
    US
    Correspondent
    Derek Purdy

    Products

    Device Name Product Code
    Electrosurgical, Cutting & Coagulation & Accessories GEI
    Generator, Lesion, Radiofrequency GXD
    System, Therapeutic, X-Ray JAD
    Ablation Catheter, Renal Denervation QYI
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation OAE
    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter OAD
    Cardiac Ablation Percutaneous Catheter LPB
    Bronchial Thermoplasty System OOY
    System, Multipurpose For In Vitro Coagulation Studies JPA
    Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation OCM

    Proprietary Names

    Paradise Cartridge Paradise Generator DiamondTemp Ablation System nGen Pump Perosphere ClotChek COOLIEF* Radiofrequency Generator (CRG) System AtriCure Synergy Ablation System

    Establishment Types

    Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Device in the United States for Export Only