Profile: Thought Technology Ltd. is a manufacturer of biofeedback and psychophysiological instruments. We produce a wide variety of instrumentation to monitor surface electromyography, electroencephalography, electrocardiology, skin conductance, temperature, blood volume pulse and respiration. We are an ISO 9001 and ISO 13485 certified company.

The company was founded in 1974, has ~40 employees and is ISO 9001, CE certified.

FDA Registration Number: 9680487
US Agent: Cindy Bruneau / Cimetra Llc.
Phone: +1-(518)-846-7606  Fax: +1-(518)-846-7617  E-Mail:

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• Aquatic Therapy, Accessories

• Assessment Equipment

• Automatic Blood Pressure Monitors

• Automotive Diagnostic Equipment

• Balance Assessment & Training Kits

• Battery-Powered Myoelectric Biofeedback Equipment

• Biofeedback & Electrotherapy

• Biofeedback Device (FDA Code: HCC / 882.5050) A biofeedback device is an instrument that provides a visual or auditory signal corresponding to the status of one or more of a patient's physiological parameters (e.g., brain alpha wave activity, muscle activity, skin temperature, etc.) so that the patient can control voluntarily these physiological parameters.

• Biofeedback Electrodes

• Biofeedback Machines

• Biofeedback Systems

• Blood Pressure Monitors

• Breath Retraining Kits

• Cardiac Monitors

• Cardiovascular Equipment Kits

• Cardiovasculars

• Chiropractic Goniometers

• Computerized Assessment Devices

• Diagnostic Equipment

• Electrical-Powered Muscle Stimulator (FDA Code: IPF / 890.5850) A powered muscle stimulator is an electrically powered device intended for medical purposes that repeatedly contracts muscles by passing electrical currents through electrodes contacting the affected body area.

• Electro Diagnostic Equipment

• Electromedical Biofeedback Devices

• Electromedical Kits, Electrodes

• Electromedical Leads

• Electromedical Muscle Stimulators

• Electromyography Device

• Electrotherapy Kits

• Functional Assessment Devices

• General Diagnostic Equipment

• Goniometers

• Hand Therapy Kits

• Heart Rate Analyzer

• Inclinometers

• Incontinence Kits

• Inspiratory Muscle Training Kits

• Medical Computer and Software (FDA Code: LNX)

• Monitoring and Diagnostic Equipment

• Muscle Stimulators, Combo UltraSound

• Muscle Strength Testers

• Neurology Monitors

• Non-Implantable Electrical Stimulator (FDA Code: KPI / 876.5320) A nonimplanted electrical continence device is a device that consists of a pair of electrodes on a plug or a pessary that are connected by an electrical cable to a battery-powered pulse source. The plug or pessary is inserted into the rectum or into the vagina and used to stimulate the muscles of the pelvic floor to maintain urinary or fecal continence. When necessary, the plug or pessary may be removed by the user. This device excludes an AC-powered nonimplanted electrical continence device and the powered vaginal muscle stimulator for therapeutic use (884.5940).

• Pain Management System

• Patient Data Management Computer

• Patient Monitor Computer

• Perineometer (FDA Code: HIR / 884.1425) A perineometer is a device consisting of a fluid-filled sack for intravaginal use that is attached to an external manometer. The devices measure the strength of the perineal muscles by offering resistence to a patient's voluntary contractions of these muscles and is used to diagnose and to correct, through exercise, uninary incontinence or sexual dysfunction.

• Rehab & Fitness Equipment

• Sleep Diagnostics Kits, Respiratory Effort Belts

• Stress Exercise Physiological Monitor

• Telemetry Systems

• Temperature Monitors