Hironic Co., Ltd., a company specializing in medical aesthetics, announced that its next-generation flagship new product 'V-RO' has received a medical device manufacturing license from the Ministry of Food and Drug Safety (MFDS).
V-RO delivers focused ultrasound energy to various skin layers such as the dermis and SMAS layer to create a number of microscopic thermal coagulation points, and then lifts as well as the traditional focused ultrasound (HIFU) function that lifts based on regeneration and recovery action. It is a lifting complex equipment that combines the high frequency (RF) function, which is another axis of the equipment.
In particular, the pen-type SD (Synergy Dotting) handpiece can be used to treat even the curved side of the face or to the detailed parts of the eye area. In addition, it is equipped with a double safety device using a skin contact sensor for safe treatment, and customized treatment according to skin depth is possible based on 6 different cartridges. In addition, through patient-specific data management, the patient's treatment history is supported without a separate chart, adding convenience.
An official from Hironic said, "V-RO is a next-generation flagship device that has received a lot of love calls under the model name of NEW DOUBLO not only in Korea but also overseas even before its launch. He continued, "I am confident that this V-ro launch will serve as a stepping stone for the second company to take off as a signal of sales and profit growth in the second half of the year."
하이로닉 영문 웹사이트로 이동합니다.
글로벌 웹사이트에는 수출용 제품으로
대한민국에서 허가하지 않은 장비 및 서비스
내용을 포함하고 있습니다. 해당 내용은
대한민국의 의료기기 광고 심의, 규제를 받지 않습니다.
It goes to the HIRONIC English website.
The Global Web Site contains equipment
and services that are not authorized by
the Republic of Korea These contents
are not subject to review and regulation
of medical devices in Korea.
하이로닉 EU 웹사이트로 이동합니다.
EU(Europe) 웹사이트의 내용은 "CE MDD 또는 CE MDR" 허가승인된 품목의 제품 정보에 관한 것으로, 대한민국의 소비자 보호를 위한 국내법 의료기기의 광고 심의, 규제를 받지 않습니다.
It goes to the HIRONIC EU website.
The contents of the EU(European) web page are about product information of items approved for "CEMDD or CEMDR" in EU countries. They are not subject to advertising deliberation and regulation of domestic law medical devices for consumer protection in Korea.