Soul Spring Centers
Powered by Wegamed Medical Technology
Medically certified devices for whole body detoxification and regeneration
At-a-Glance Benefit Summary
State-of-the-art medical technology identifies hidden root causes of disease traditional lab tests may miss.
Provides immediate relief
Uncovers the root causes
Access overall balance and harmony in your wellbeing
Medically certified devices
Gain in-depth insights
Applicable for all age groups including senior citizens
Experience Our State-of-the-Art Medical Devices
Every Soul Spring center applies proven protocols we developed for expert use of Wegamed medtech.
Diagnosis: We Go Beyond Traditional Lab Testing
State-of-the-art technology identifies hidden root causes of disease normal lab tests may miss.
Therapies: Immediate Results with Lasting Impact
We are thrilled to have brought the Wegamed legacy into our growing family for best-in-class bio-wellness solutions.
Wegamed and Soul Spring Have Partnered since 2019
We are thrilled to have brought the Wegamed legacy into our growing family for best-in-class bio-wellness solutions
The Wegamed Story: How Have We Evolved?
Following his career as a semi-professional soccer player and swimmer, Dr. Peter Mölleney merged his passion for sports with his family legacy in the field of medicine to create Wegamed GmbH, headquartered in Essen.
A fifth-generation physician with his own naturopathic practice, Dr. Mölleney utilized his training in traditional and alternative medicine, along with psychotherapy, to develop Wegamed’s innovative med tech devices specializing in detoxification and regeneration therapies at the cellular level. Under the direction of Dr. Mölleney, Wegamed carries on the tradition of Vega Grieshaber KG collaborating with engineers and research institutions to develop new devices for effective diagnoses and non-invasive therapies.
Backed by 25+ years of research and clinical trials, Wegamed’s Diagnostic, Therapeutic and Wellness Devices are approved for medical use in Germany (DIMDI) and several other countries. The devices are Class 2A CE-marked, clinically approved and FDA registered.
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