THE ONLY COMPRESSION TECHNOLOGY IN THE WORLD THAT CAN ASSIST WITH RECOVERY FROM HAMSTRING, GROIN, HIP, AND PELVIC INSTABILITY

Endorsements and Accreditation

ACA

The Australian Chiropractors Association (ACA) is the peak body representing chiropractors.

An underlying principle of chiropractic is “healthy spine, healthier life”. By offering expert drug-free spinal health care and lifestyle advice, chiropractors help Australians lead and maintain healthy lives.

With approximately 3,000 members, the ACA is the largest chiropractic health body in Australia.

Supacore products have been evaluated by the ACA product evaluation Committee and comply with the products specifications.

 “I have personally been using and referring my patients to the Suparcore range since I was introduced to the product.
Having the ability to direct patients to an amazing product that is used by some of the biggest soccer clubs in Europe, as well as AFL and NRL clubs is amazing. Be it for the weekend warrior, semi or professional athlete to their amazing pre and post pregnancy recovery shorts, you can have confidence in using Supacore products for you and your patients”.

- Dr Craig Skicko,B. App Sc(CM-CHIRO) M Clin Chiro Victoria.

 

TGA Health Safety Regulation

 

As part of the Department of Health, the TGA safeguards and enhances the health of the Australian community through effective and timely regulation of therapeutic goods.

The TGA regulates therapeutic goods through pre-market assessment, post-market monitoring and enforcement of standards, licensing of Australian manufacturers and verifying overseas manufacturers' compliance with the same standards as their Australian counterparts.

Supacore Coretech ® is listed as a Medical device class 1.  ARTG entry 207539.

 

 

CE Marking

 

CE Marking is the symbol as shown on the top of this page. The letters "CE" are the abbreviation of French phrase "Conformité Européene" which literally means "European Conformity". The term initially used was "EC Mark" and it was officially replaced by "CE Marking" in the Directive 93/68/EEC in 1993. "CE Marking" is now used in all EU official documents.

CE Marking on a product is a manufacturer's declaration that the product complies with the essential requirements of the relevant European health, safety and environmental protection legislation, in practice by many of the so-called 

Supacore Coretech ® is listed as a Medical device class 1.  

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