Stellartech Research Corp.

FDA Device Registration & Listing · Milpitas, CA, US · Registration 3010653929

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3010653929
FEI Number
3010653929
Entity Name
Stellartech Research Corp.
City/State/Country
Milpitas, CA, US
Establishment Address
560 Cottonwood Dr, Milpitas, CA 95035, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
STELLARTECH RESEARCH CORP. (Owner Number: 9022137)
Owner / Operator Contact Address
560 Cottonwood Drive, --, Milpitas, CA 95035, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

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

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2013-02-01
GXD Generator, Lesion, Radiofrequency Neurology Class 2 882.4400 2013-02-01
JAD System, Therapeutic, X-Ray Radiology Class 2 892.5900 2013-02-01
QYI Ablation Catheter, Renal Denervation Unknown Class 3 N/A 2023-11-20
OAE Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation Unknown Class 3 N/A 2021-03-10
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2013-02-01
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter Unknown Class 3 N/A 2021-11-05
OAE Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation Unknown Class 3 N/A 2021-11-05
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2021-11-05
OOY Bronchial Thermoplasty System Unknown Class 3 N/A 2013-02-01
JAD System, Therapeutic, X-Ray Radiology Class 2 892.5900 2013-02-01
JPA System, Multipurpose For In Vitro Coagulation Studies Hematology Class 2 864.5425 2025-12-15
GXD Generator, Lesion, Radiofrequency Neurology Class 2 882.4400 2020-02-27
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter Unknown Class 3 N/A 2014-07-30
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2014-07-30

Official Correspondent

Derek Purdy

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

STELLARTECH RESEARCH CORP.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17
K002257 Tecno Instruments (Pvt.) , Ltd. TECNO DISPOSABLE FINGERSWITCH PENCIL, MODEL 150-100 2000-10-19
K193591 Bowa-Electronics GmbH & Co. KG ARC 400 2020-04-02
K192128 Sutter Medizintechnik GmbH Sutter Arrowtip Monopolar Electrodes 2019-10-04

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826
Z-0664-2020 Abbott Medical 2
Radiofrequency Grounding Pad, REF RF-DGP-L
Z-0001-2018 Carl Zeiss Meditec AG Rudolf-Eber-Str. 11 Oberkochen Germany 2
Carl Zeiss INTRABEAM PRS 500, product #304534-0000-500. The firm name on the label is Carl Zeiss Meditec AG, Jena, Germany. The INTRABEAM System is indicated for radiation therapy treatments
Z-0032-06 BIOMERIEUX, INC. 2
VeriCal Calibrator Set
Z-0042-05 Dade Behring Inc. Rte 896, Glasgow Business Community 2
DispoSystem for BCT System.Model number OVFR03. Multipurpose System for in vitro coagulation studies.

Similar Registrations

Registration Number Establishment Name Location
3007353760 ENERGIST LIMITED Swansea, GB
3005064998 RDI INC. Mount Kisco, NY, US
3020623326 TRIWORKS GROUP S.R.L. Palata Campobasso, IT
3012616488 BRERA MEDICAL INCORPORATED Northborough, MA, US
3012940012 Sutter Medical Technologies USA Inc. Alpharetta, GA, US
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010653929. Last updated year: 2026. Please use registration number 3010653929 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.