Pioneering Aesthetic
Medical Innovation
BRITZMEDI has evolved from a specialized R&D institute into a global medical device manufacturer, holding FDA clearance and Venture Enterprise certification. We are committed to researching sustainable beauty for everyday life through innovative aesthetic devices.
Company Overview
BRITZMEDI Co., Ltd.
(주)브리츠메디
Shin Jae Lee
Appointed December 2, 2025
October 23, 2017
1F, 2, Gisan-ro 87beon-gil, Hwaseong-si, Gyeonggi-do, Republic of Korea
Manufacturer of Medical Devices, R&D, Wholesale & Retail
Our Philosophy
"Beyond developing aesthetic devices, we are committed to researching sustainable beauty for everyday life."
Intellectual Property
Company History & Milestones
From a specialized R&D institute to a global medical device manufacturer with FDA clearance.
Company Establishment
Established BRITZMEDI Co., Ltd. and certified as a Company-Affiliated Research Institute
GMP Certification
Obtained GMP (Good Manufacturing Practice) Certification from MFDS
FDA Clearance & ISO Certification
Acquired FDA 510(k) clearance for TORR RF (K212561) and ISO 13485:2016 certification
Venture Enterprise Re-designation
Re-designated as 'Venture Enterprise' (R&D Type), valid until June 2028
LUMINO WAVE Launch
Scheduled launch of next-generation LUMINO WAVE device (H2 2026)
Research & Development Capabilities
BRITZMEDI operates as a technology-intensive company with a strong focus on intellectual property to secure competitive advantages in the aesthetic medical field.
Core Technologies
Convergence Therapy
Technology combining Ultrasound and Laser to maximize skin penetration
Applied to: LUMINO WAVEMulti-Wave RF Technology
Patented RF thermal systems with segmented electrode designs
Applied to: TORR RFTransdermal Delivery
Acoustic cavitation technology for deep skin absorption
Applied to: ULBLANC (i-Booster)Manufacturing & OEM/ODM Capabilities
BRITZMEDI possesses full-cycle manufacturing capabilities and offers development services for global partners.
Manufacturing Infrastructure
Our company operates a dedicated manufacturing facility in Hwaseong-si, authorized by the Ministry of Food and Drug Safety.
OEM/ODM Readiness
Officially registered with the U.S. FDA as a Contract Manufacturer, verifying our capability to produce medical devices meeting stringent U.S. standards.