LINEMASTER SWITCH CORP.

FDA Device Registration & Listing · WOODSTOCK, CT, US · Registration 3001592626

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
3001592626
FEI Number
3001592626
Entity Name
LINEMASTER SWITCH CORP.
City/State/Country
WOODSTOCK, CT, US
Establishment Address
29 PLAINE HILL RD, WOODSTOCK, CT 06281, US
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
LINEMASTER SWITCH CORP. (Owner Number: 9080742)
Owner / Operator Contact Address
29 PLAINE HILL ROAD, --, Woodstock, CT 06281, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

6700-313-003 Coag single foot pedal MFSW1 Neuwave LS0010 Ligasure 2-Pdeal footswitch LS0300 FTSW SGLE Ligasure E6019 GEM Bipolar footswitch A803 Footswitch Foot pedal RIO Instrumentation 6700-313-002 Coag only dual foot pedal FSW11 Stanley Footswitch Round Bipolar Footswitch Maestro Foot Switch RF Generator Accessory FS-1 MetriQ Foot Switch RF Footswitch RIO Instrumentation SMARTFREEZETM Cryo-Console Foot Switch Maestro Foot Switch AR 9800-F Synergy Footswitch FSW11 323863 (single-pedal auxiliary footswitch) and 323864 (dual-pedal auxiliary footswitch) AES-FCE Arthroscopic energy foot control, extension ABC Foot Switch 60-8470-001 ABC Foot Switch 60-8475-001 IR WIRELESS FOOT SWITCH PulseSelect™ Pulsed Field Ablation (PFA FT6009 Bipolar resection footswitch E6008 Footswitch Standard The ETHICON™ Total Energy System FT6003 3-PDL Footswitch LF0500 LGSR SGL PDL Footswitch E6009 Footswitch 1400JJ Monopolar Footswitch 1450J Bipolar Footswitch Maestro Foot Switch RIO Instrumentation Medtronic Nitron Footswitch RIO Intrumentation 5500-006-000 Sonopet iQ Ultrasonic Aspirator System 5500-008-000 Sonopet iQ Ultrasonic Aspirator System 5500-007-000 Sonopet iQ Ultrasonic Aspirator System 1910-2002 footswitch AR-8310 APS II Footswitch, Standard Core Footswitch NSE Footswitch Valleylab Monopolar Footswitch AES-WFC Arthroscopic energy wireless foot control AES-FC Arthroscopic energy foot control Rythmia Mapping System Foot Switch AR-6483 Dual Wave Foot Control

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 2020-03-24
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2018-10-15
NEY System, Ablation, Microwave And Accessories General, Plastic Surgery Class 2 878.4400 2025-08-01
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2017-01-26
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2017-01-26
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2024-09-19
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2022-06-07
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2017-07-12
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2020-03-24
HGI Electrocautery, Gynecologic (And Accessories) Obstetrics/Gynecology Class 2 884.4120 2016-04-13
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2016-04-13
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2016-04-13
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2020-11-12
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2016-04-13
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter Unknown Class 3 N/A 2016-04-13
GXD Generator, Lesion, Radiofrequency Neurology Class 2 882.4400 2019-06-19
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter Unknown Class 3 N/A 2016-04-13
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2021-04-27
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2017-07-12
OAE Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation Unknown Class 3 N/A 2023-09-21
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2016-04-13
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2021-05-11
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2018-02-16
HGI Electrocautery, Gynecologic (And Accessories) Obstetrics/Gynecology Class 2 884.4120 2018-02-16
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2018-02-16
GAT Suture, Nonabsorbable, Synthetic, Polyethylene General, Plastic Surgery Class 2 878.5000 2016-04-13
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2016-04-13
MAI Fastener, Fixation, Biodegradable, Soft Tissue Orthopedic Class 2 888.3030 2016-04-13
NAY System, Surgical, Computer Controlled Instrument Gastroenterology, Urology Class 2 876.1500 2026-06-01
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2026-06-01
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2017-09-19
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2016-08-30
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2006-04-20
DQK Computer, Diagnostic, Programmable Cardiovascular Class 2 870.1425 2017-04-05
QZI Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation Unknown Class 3 N/A 2023-12-20
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2017-01-26
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2025-02-19
HGI Electrocautery, Gynecologic (And Accessories) Obstetrics/Gynecology Class 2 884.4120 2025-02-19
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2025-02-19
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2017-01-26
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2019-05-28
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2016-04-13
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2017-07-12
LPB Cardiac Ablation Percutaneous Catheter Unknown Class 3 N/A 2024-12-17
OLO Orthopedic Stereotaxic Instrument Neurology Class 2 882.4560 2017-07-12
LFL Instrument, Ultrasonic Surgical Unknown Class U N/A 2020-03-24
HTY Pin, Fixation, Smooth Orthopedic Class 2 888.3040 2015-01-21
HWE Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment General, Plastic Surgery Class 1 878.4820 2020-10-16
HBE Drills, Burrs, Trephines & Accessories (Simple, Powered) Neurology Class 2 882.4310 2020-04-13
BWA Unit, Electrosurgical And Coagulation, With Accessories General, Plastic Surgery Class 2 878.4400 2021-03-01
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2017-09-19
DQK Computer, Diagnostic, Programmable Cardiovascular Class 2 870.1425 2018-10-23
HRX Arthroscope Orthopedic Class 2 888.1100 2020-05-11

Official Correspondent

Deborah Kettlety

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LINEMASTER SWITCH 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-0027-2024 Bard Peripheral Vascular Inc 2
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Z-0028-2013 Remington Medical Inc. 2
Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle biopsies of the prostate. The needles are compatible with the Bard Magnum biopsy instrument. The needles have an echogenic tip for accurate placement under ultrasound guidance and centimeter markings along the cannula to facilitate depth placement.
Z-0042-2014 Atossa Genetics, Inc. 2
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Sample Kits & Clarity Patient Sample Kits Instrument, Biopsy. The MASCT System Kit, Patient Sample Kits, or the Nipple Aspirate Fluid Laboratory Kit has the following codes: PRODUCT CODE: AG-MASCT; AG-FC5; DTG-MASCT, DTG-FC5, and NRLBH-5. PART NUMBER: 9002513; 9002513MD; 9002528; 9002528MD; 9002587; 9002614; and 9002717MD. THE MASCT SYSTEM KIT CONSISTS OF: 1. MASCT Breast Pump; 2. Instructions for Use (IFU); 3. Heating Pad; 4. Timer; 5. Saccomono's Fixative; 6. Nu Prep Gel; 7. Welcome and Training Materials Coversheet; 8. MASCT System Order Form; 9. ForeCYTE Training Video DVD; 10. MASCT System Instructions with pictures - pink; THE PATIENT SAMPLE KIT CONSISTS OF: 1. Two (2) flower assemblies (e.g., filter, filter retainer, and filter holder); 2. Instructions for Use (IFU); 3. Two (2) specimen collection devices; 4. Two (2) breast bags for transporting the specimen collection container; 5. Barcode labels; 6. Saccomono's Fixative; 7. Nu Prep Gel; 8. MASCT System package insert; 9. ForeCYTE Test Requisition Form; 10. Patient Information Sheet; 11. Atossa Patient Information; 12. FED EX Clinical PAK; 13. MASCT System Order Form; 14. FED EX Pouch; 15. FED EX Airbill; Product Usage: The MASCT Device is intended for use in the collection of nipple aspirate fluid for cytological testing. The collected fluid can be used in the determination and/or differentiation of normal versus premalignant versus malignant cells.
Z-0044-2018 Bard Peripheral Vascular Inc 2
BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3001592626. Last updated year: 2026. Please use registration number 3001592626 when referencing this establishment in official correspondence.
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