Sisram Medical Ltd (HKG: 1696), a China-based global wellness group offering Energy-Based Devices (EBDs), injectables, and other complementary solutions, announced on Monday that China's National Medical Products Administration (NMPA) had formally accepted the registration application for Profhilo's facial indication in September.
The company claims that this milestone marks a significant step toward introducing the product to the Chinese market.
According to Sisram, Profhilo is a high-concentration sodium hyaluronate product featuring a BDDE-free formulation developed using patented NAHYCO technology. Through biostimulation and deep skin hydration, the product seeks to promote collagen and elastin production, aimed at helping improve skin texture, firmness, and elasticity. With its differentiated technology and unique product attributes, Profhilo is claimed to hold a distinct competitive advantage in the medical aesthetics skin rejuvenation segment.
Sisram currently holds exclusive distribution rights for Profhilo across several markets, including Israel, India, and Thailand. In Thailand, Profhilo is said to have maintained robust growth momentum, gaining widespread acceptance among leading medical aesthetics clinics and experienced practitioners. Building on this success, Sisram has introduced combination treatment protocols integrating Profhilo with its Soprano series of EBD platforms, leveraging synergies between its EBD and injectables businesses to deliver differentiated treatment solutions. It adds that these proven commercial practices and accumulated clinical expertise provide valuable insights and a foundation for Profhilo's planned entry into the Chinese market.
Alongside the ongoing registration process, Sisram has initiated comprehensive commercialisation preparations for Profhilo in China, covering market positioning, channel strategy, medical education, end-user engagement, and operational planning.
Natera secures FDA Breakthrough Device designation for multi-cancer early detection assay
Okami Medical receives FDA approval for expanded indication of LOBO Vascular Occluder
Oxurion in talks to acquire Eclevar's MedTech CRO business and assets
FDA Advisory Committee votes in favour of GRAIL's Galleri multi-cancer early detection test
Insmed's ARIKAYCE sNDA granted priority review by FDA
ProBio and Kun Tuo collaborate to deliver integrated CDMO-CRO solutions for advanced therapies
Myosin Therapeutics chosen for 2026-2027 NCI Investor Initiatives Showcase
Medtronic receives FDA clearance for LigaSure RAS Maryland instrument on Hugo system
Aptar and Aceso Therapeutics partner to advance inhaled cystic fibrosis therapy
Immuron signs US distribution deal for PROIBS
Tempus announces receipt of FDA clearance for AI pulmonary hypertension detection product
Pulnovo Medical commences enrolment in PULSE-LHD IDE clinical trial
Implantica's RefluxStop receives US FDA approval
Sectra to provide Education Portal to Loyalist College for medical imaging training