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LD TECHNOLOGY, LLC, a U.S. Company based in Florida, developed state of the art, computer-based technologies that provide new applications employable in the fields of noninvasive, bioelectrical impedance monitoring and plethysmography.

The LD TECHNOLOGY enterprise comprises medical doctors, a programming engineer, software developers, physicists, mathematicians, and statisticians who support its leadership in the field in biosensor technology.

 
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LD TECHNOLOGY products include:
1. The EIS System (a.k.a. “EIS”; Electro Interstitial Scan): a unique biosensor with specific intended uses:

>> EIS-BF Devices Sec. 882.5050 Biofeedback device.
(a)Identification. 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. 510k exemption ( Listed and registered FDA Class II )
>> EIS-BC Measurement of the galvanic Skin responses, nutrition, and estimated parameters of body composition (EC Marks Class II a as a medical device in European marketplace )
>>EIS system monitoring of treatments for select diseases and as an adjunct to conventional diagnosis of ADHD children ( EC Mark Class IIa, as a medical device in European, Asian, and South American, Canada (Class II) and Australian marketplaces.

2. E.S. Teck/PEMS (a.k.a. 'EST'; Electro Sensor Teck; EC marks, Health Canada (Class III) , and FDA 510k Clearance ): a single, unique hardware/software computerized system designed to study heart rate variability (HRV), SpO2 and photoelectric plethysmography .

3. E.S Teck Complex software: :Health Care solution. All-in-one software to manage a combination of the 4 technologies. (EC Mark Class IIa as a medical device in European, Asian, South American and Australian marketplaces)

4. ITM (Impedance Tomography Mammographic), a relatively small, simple-to-use, yet powerful device intended for the investigation of mammary glands and use as an adjunct to mammography in patients who have equivocal mammographic findings within ACR BI-RADSTM categories 3 or 4. It is not, however, intended for use in cases with clear mammographic or non-mammographic biopsy indications. This technology provides the radiologist with additional information to guide any biopsy recommendation.(EC mark Class IIa as a medical device in European marketplace)

 
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>>US Market: ES TECK PEMS
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