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Home
Biofield Technology Products
- THERA WELLNESS® Device
- THERA WELLNESS® Vitalyzer
Wellness Therapies
Animal Care
Meet Our Team
Find a Provider
Resources Hub
Shop

Home
Biofield Technology Products
- THERA WELLNESS® Device
- THERA WELLNESS® Vitalyzer
Wellness Therapies
Animal Care
Meet Our Team
Find a Provider
Resources Hub
Shop

Home
Biofield Technology Products
- THERA WELLNESS® Device
- THERA WELLNESS® Vitalyzer
Wellness Therapies
Animal Care
Meet Our Team
Find a Provider
Resources Hub
Shop

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Accessories
Thera
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Functional Circuits & Reflex Zones Poster

$75.00

Functional circuits & Reflex zones poster

Glass insertions (50 ml), 2 pcs.

$24.00

50mL-glass-beaker

Goldfinger applicator with teflon handle

$165.00

goldfinger

HERBS (GREEK REMEDIES)

$260.00

well_being_logo

Honeycomb with base – new style

$201.00

square252BG0918

Honeycomb with base – original style

$168.00

square252BG0901

Lid for cup applicator

$21.00

TH442-Lid for cup applicator

Long teflon dental test applicator

$158.00

TH417-Long teflon dental test applicator

Lower part honeycomb – new style replacement

$92.00

square2BG0921

Magnetic depth probe

$443.00

Magnetic-Depth-Probe

Magnetic knob applicator – 32 mm

$80.00

THERA brass knob applicator

Memory patches / chips (100 pcs.)

$308.00

Thera Chips

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+12404421919

10411 Motor City Drive, Ste. 615 Bethesda, MD 20817

Disclaimer: Although the technology behind THERA WELLNESS® products — including the THERA WELLNESS® device and the THERA WELLNESS® Vitalyzer — has been evolving for over 40 years, its connection to health and wellness has not been established or demonstrated to the extent required by the U.S. Food and Drug Administration (FDA) for medical devices. THERA WELLNESS® products are not intended to diagnose, cure, mitigate, prevent or treat any disease or medical condition. They are intended, alongside a healthy diet and lifestyle, to support general wellbeing. THERA WELLNESS® products are intended for general wellness use consistent with FDA’s guidance “General Wellness: Policy for Low Risk Devices,” docket FDA-2014-N-1039, issued January 6, 2026.

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