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THE 2014 & 2015 ``BEST OF CLASS`` EMERGING TECHNOLOGY AWARD

PROPEL’s Excellerator Series received the coveted “Best of Class” Technology Award from the Pride Institute and was praised as “a game changer in orthodontics,” that reflects “value for the patient outcome and real-world impact” for 2 consecutive years, 2014 and 2015…

 

Reference link – 2015  
Read up more on the article – 2014    PDF Cover  

main_award_placeholder_02

THE 2014 & 2015 ``BEST OF CLASS`` EMERGING TECHNOLOGY AWARD

PROPEL’s Excellerator Series received the coveted “Best of Class” Technology Award from the Pride Institute and was praised as “a game changer in orthodontics,” that reflects “value for the patient outcome and real-world impact” for 2 consecutive years, 2014 and 2015…

 

Reference link – 2015  
Read up more on the article – 2014    PDF Cover  

main_award_placeholder_02

THE 2014 & 2015 ``BEST OF CLASS`` EMERGING TECHNOLOGY AWARD

PROPEL’s Excellerator Series received the coveted “Best of Class” Technology Award from the Pride Institute and was praised as “a game changer in orthodontics,” that reflects “value for the patient outcome and real-world impact” for 2 consecutive years, 2014 and 2015…

 

Reference link – 2015  
Read up more on the article – 2014  
PDF Cover – 2014  

LICENSING FOR FDA & HSA. FDA – PROPEL devices are a class 1, FDA registered devices. The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products. PROPEL devices are also HSA approved. The HSA’s Health Products Regulation Group ensures that medicines, medical devices and other health products available in Singapore meet appropriate and acceptable standards in quality, safety and efficacy.

LICENSING FOR FDA & HSA. FDA – PROPEL devices are a class 1, FDA registered devices. The Food and Drug Administration (FDA or USFDA) is a federal agency of the United States Department of Health and Human services, one of the United States federal executive departments. The FDA is responsible for protecting and promoting public health through the regulation and supervision of food safety, tobacco products, dietary supplements, prescription and over-the-counter pharmaceutical drugs, vaccines, biopharmaceuticals, blood transfusions, medical devices, electromagnetic radiation emitting devices (ERED), cosmetics, animal foods & feed and veterinary products. PROPEL devices are also HSA approved. The HSA’s Health Products Regulation Group ensures that medicines, medical devices and other health products available in Singapore meet appropriate and acceptable standards in quality, safety and efficacy.