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2025.11.27
[Bio in Focus] Mezoo, Connecting the Ward with a Single Patch


Implementing a “One-Patch System” with On-Device Technology

 

Strategic partner Dong-A ST targets the domestic market

 

Application for KOSDAQ preliminary listing review in October… IPO planned for next year

 

A hidden powerhouse in digital healthcare, armed with strong on-device technology and a partnership with Dong-A ST, is preparing for its KOSDAQ debut. The company is Mezoo, developer of a mobile ambulatory remote patient monitoring (aRPM) solution.

 

A mobile remote patient monitoring solution is a system that transmits patients’ biosignals to a hospital monitoring center using patches attached to the body along with smartphones and other devices. It enables real-time delivery of biosignals such as electrocardiograms and respiration even when patients move inside or outside hospital wards or remain at home. This is currently one of the hottest areas in the domestic digital healthcare sector.

 

aRPM “Mezoo” Challenges Entry into KOSDAQ

 

Mezoo is a digital healthcare company co-founded in 2018 by CEO Jung-hwan Park, a graduate of Yonsei University’s Department of Biomedical Engineering, along with three biomedical engineering PhDs—Seong-pil Cho, Mi-hye Song, and Jae-yeon Shin.

 

The company’s core proprietary technologies include “biomedical telemetry,” which wirelessly and stably transmits biosignals such as ECG and respiration from patients and refines them into clinically usable data, and the “HCF framework,” which integrates overall hospital workflows. Based on these technologies, Mezoo has commercialized a mobile remote patient monitoring solution.

 

Mezoo’s solution enables 24-hour monitoring of an entire ward by linking data from a low-power, miniaturized patch-type electrocardiograph, HiCardi, attached to the patient’s chest, with smartphones, the cloud, and centralized monitoring software (LiveStudio).


https://news.bizwatch.co.kr/article/healthcare/2025/11/26/0019

 

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하이카디® 시스템은 인허가에 따라 신생아, 소아, 청소년, 18세 이상 환자의 ECG 데이터를 측정하여 부정맥을 진단하는 의료기기로서 의료전문가가 사용하도록 설계되었습니다. 한국 KFDA로부터 의료기기 2등급 인증을 받았습니다. 유럽의료기기 지침(2007/47/EC에 따라 개정된 MDD 93/42/EEC)에 따라 준수된 Class IIb (CE2265). 의료기기 제품으로 CE 승인되었습니다. 미국 FDA는 Class II 510K로 승인 완료 예정입니다.

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