Data / Medical devices / United States / Linemaster Switch Corp.

Linemaster Switch Corp.: FDA-registered device maker in Woodstock, CT, United States, 1 510(k) clearance

Name: Linemaster Switch Corp. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Linemaster Switch Corp. is registered with the FDA (registration 3001592626) in Woodstock, CT, United States. It lists 24 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 20, 2006. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3001592626
Address: 29 Plaine Hill RD, Woodstock, CT, United States, 06281
Owner or operator: LINEMASTER SWITCH CORP. (9080742)
Roles: Contract manufacturer, Manufacturer
First device listed: April 20, 2006
Registered through: 2026
Brand names listed: 1400JJ Monopolar Footswitch, 1450J Bipolar Footswitch, 1910-2002 footswitch, 323863 (single-pedal auxiliary footswitch) and 323864 (dual-pedal auxiliary footswitch), 5500-006-000 Sonopet iQ Ultrasonic Aspirator System, 5500-007-000 Sonopet iQ Ultrasonic Aspirator System, 5500-008-000 Sonopet iQ Ultrasonic Aspirator System, 6700-313-002 Coag only dual foot pedal and more

Devices it lists

Device	Product code	Class	Role	Source
Arthroscope	HRX	2	Contract manufacturer	accessdata.fda.gov
Cardiac Ablation Percutaneous Catheter	LPB	3	Contract manufacturer	accessdata.fda.gov
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation	OAE	3	Contract manufacturer	accessdata.fda.gov
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter	OAD	3	Contract manufacturer	accessdata.fda.gov
Computer, Diagnostic, Programmable	DQK	2	Contract manufacturer	accessdata.fda.gov
Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece	ERL	2	Contract manufacturer	accessdata.fda.gov
Drills, Burrs, Trephines & Accessories (Simple, Powered)	HBE	2	Contract manufacturer	accessdata.fda.gov
Electrocautery, Gynecologic (And Accessories)	HGI	2	Contract manufacturer	accessdata.fda.gov
Electrosurgical, Cutting & Coagulation & Accessories	GEI	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Endoscope, Neurological	GWG	2	Contract manufacturer	accessdata.fda.gov
Fastener, Fixation, Biodegradable, Soft Tissue	MAI	2	Contract manufacturer	accessdata.fda.gov
Generator, Lesion, Radiofrequency	GXD	2	Contract manufacturer	accessdata.fda.gov
Instrument, Biopsy	KNW	2	Contract manufacturer	accessdata.fda.gov
Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/Attachment	HWE	1	Contract manufacturer	accessdata.fda.gov
Instrument, Ultrasonic Surgical	LFL	U	Contract manufacturer	accessdata.fda.gov
Laser, Ophthalmic	HQF	2	Contract manufacturer	accessdata.fda.gov
Nasopharyngoscope (Flexible Or Rigid)	EOB	2	Contract manufacturer	accessdata.fda.gov
Orthopedic Stereotaxic Instrument	OLO	2	Contract manufacturer	accessdata.fda.gov
Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation	QZI	3	Contract manufacturer	accessdata.fda.gov
Pin, Fixation, Smooth	HTY	2	Contract manufacturer	accessdata.fda.gov
Suture, Nonabsorbable, Synthetic, Polyethylene	GAT	2	Contract manufacturer	accessdata.fda.gov
System, Ablation, Microwave And Accessories	NEY	2	Contract manufacturer	accessdata.fda.gov
System, Surgical, Computer Controlled Instrument	NAY	2	Contract manufacturer	accessdata.fda.gov
Unit, Electrosurgical And Coagulation, With Accessories	BWA	2	Contract manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
March 20, 2006	K053510	IR WIRELESS FOOT SWITCH	GEI	Substantially Equivalent	Linemaster Switch Corp.	accessdata.fda.gov

Compare with other makers

Updated March 20, 2006. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.