Created with Pixso. Home Created with Pixso. About Us Created with Pixso. Factory Tour

Factory Tour

Production Line

Shenzhen Weideshi Technology operates 6 fully standardized production lines dedicated to aesthetic equipment manufacturing, in strict compliance with ISO 9001 quality management system and ISO 13485 medical device standards.

We carry out a full-process quality inspection system, including incoming material testing, semi-finished product debugging, finished machine performance verification, aging test and safety assessment. Every device including diode laser hair removal, HIFU, IPL, RF and slimming machines passes rigorous multi-round checks before delivery, ensuring stable quality, safety and full compliance with global market requirements.

company.img.alt
company.img.alt
company.img.alt
company.img.alt
company.img.alt
company.img.alt
company.img.alt
company.img.alt
company.img.alt
OEM/ODM

Shenzhen Weideshi Technology operates 6 fully standardized production lines dedicated to aesthetic equipment manufacturing, in strict compliance with ISO 9001 quality management system and ISO 13485 medical device standards.

We carry out a full-process quality inspection system, including incoming material testing, semi-finished product debugging, finished machine performance verification, aging test and safety assessment. Every device including diode laser hair removal, HIFU, IPL, RF and slimming machines passes rigorous multi-round checks before delivery, ensuring stable quality, safety and full compliance with global market requirements.

R&D

Shenzhen Weideshi Technology houses a professional in-house R&D center composed of multidisciplinary experts with extensive experience in optoelectronic technology, medical aesthetics and electronic engineering. Our R&D team focuses on continuous innovation and core technology upgrading for a full range of aesthetic devices, including diode laser hair removal, HIFU, IPL, E-light, RF, long-pulse Nd:YAG laser, fractional laser, vital injection and body slimming machines.

We follow strict R&D processes fully compliant with ISO 9001 and ISO 13485 medical device standards. Every new technology and product goes through complete prototype development, precision performance testing, clinical effect verification and multi-dimensional safety assessment to ensure high efficacy, stable output and global regulatory compliance.

Our robust R&D capability supports tailored technical development, functional optimization and exclusive product design for global partners, enabling us to launch market-leading devices that fit regional demands and industry trends. With sustained investment in innovation, we continuously enhance product competitiveness and provide reliable, forward-looking technical support for long-term global partnerships.

Contact Us