INTRODUCING THE BIOPTRON FAMILY

All three BIOPTRON devices emit identical medical grade polarized light,­ they differ only in the treatment surface area, size and design.

  FEATURES OF BIOPTRON DEVICES 

SWISS MADE MEDICAL DEVICES WITH PATENTED TECHNOLOGY
NATURAL, SAFE MEDICAL THERAPY
EASY, SHORT & PAINLESS TREATMENT
NO KNOWN SIDE EFFECTS

BIOPTRON DEVICES: BIOPTRON devices are medical devices used in hospitals, specialist institutions, wellness and sports centers and as well as at home.

BIOPTRON LIGHT THERAPY SYSTEM: Suitable for everybody. It can be used to treat a wide range of medical conditions. Easy to use, painless and time-effective, it has no known side effects.

INNOVATIVE TECHNOLOGY: BIOPTRON devices have an innovative technology and are designed to be user-friendly.

FLOOR STANDS: Each device has floor stands that allow optimal positioning and a convenient treatment of the whole body to meet everyone’s needs.

In this way, each part of the body can be easily treated so that the user can just relax and enjoy the treatment. Differing only in size and design, all three devices have the same physical light characteristics and thus have the same beneficial effect on the human body.

SWISS-MADE: All BIOPTRON Light Therapy devices are made in Switzerland by BIOPTRON AG.

BIOPTRON AG: A Swiss company, founded in 1988, that became part of the Zepter Group in the mid-1990s. Distinguished results in the field of light therapy stem from the scientific research, experience and expertise potential of the Zepter Group. These findings have been continuously implemented in the production of the BIOPTRON Light Therapy System.

BIOPTRON APPLICATION

BIOPTRON devices can be used to treat:

BIOPTRON LIGHT THERAPY: A FAST, EASY, SAFE AND EFFECTIVE TREATMENT

Certificate for
Quality Assurance
(EN ISO 9001)

Certificate for
Quality Assurance
(EN ISO 13485)

Certificate for the
Quality Assurance
System (directive
93/42/EEC)

CERTIFICATES

BIOPTRON AG in-house laboratories are constantly engaged in the testing and optimisation of BIOPTRON devices in line with the latest scientific studies carried out by independent institutions. Simultaneously, BIOPTRON devices are further certified by accredited, independent testing institutions. Our business processes, including R&D, supplier evaluation, the supply of components to production, ongoing inspections and the product itself, comply with the European Community medical directive 93/427EEC, as well as with specific local market regulations.

FDA
510 (k) clearance for pain

For further information visit "510(k) Premarket Notification Database" Our 510(k) No: K032216