Tangji Medtech Files Hong Kong IPO for First NMPA-Approved Endoscopic Obesity Device

Tangji Medtech Files Hong Kong IPO for First NMPA-Approved Endoscopic Obesity Device

Hangzhou Tangji Medical Technology Co., Ltd. has filed its IPO prospectus with the Hong Kong Stock Exchange, targeting a main board listing to capitalize on its position as China’s pioneer in endoscopic obesity treatment. The company’s flagship Gastric Bypass Stent System (GBS), first approved by NMPA in January 2024 as a Class III innovative medical device, offers a minimally invasive alternative to bariatric surgery for weight loss and metabolic disease management.

Transaction Overview

ElementDetail
CompanyHangzhou Tangji Medical Technology Co., Ltd.
Listing VenueHong Kong Stock Exchange (Main Board)
Filing DateWeek of 09 Feb 2026
Founded2016
SectorMedical devices – obesity and metabolic disease
Use of ProceedsExpected to fund commercialization, R&D pipeline, and manufacturing scale-up

Flagship Product: Gastric Bypass Stent System (GBS)

FeatureGBS SpecificationClinical Value
Design InspirationRoux-en-Y Gastric Bypass (RYGB) surgeryMimics metabolic benefits of gold-standard bariatric procedure
DeliveryEndoscopic, minimally invasiveNo abdominal incisions; reduced recovery time vs. surgery
Regulatory StatusClass III innovative medical device (NMPA, Jan 2024)First device in China approved for endoscopic obesity treatment
MechanismStent-based gastric bypass simulationRestricts food intake and alters nutrient absorption pathways
Target PopulationObese patients (BMI ≥28) with metabolic comorbiditiesBridge between lifestyle intervention and invasive surgery

Market Context & Strategic Positioning

FactorMarket Implication
China Obesity Epidemic>50% of adults overweight/obese; 120 million with BMI ≥28; bariatric surgery penetration <1% due to invasiveness and cost
Endoscopic Bariatrics GapNo approved devices prior to GBS; massive unmet need between drugs (GLP-1 shortages) and surgery
GLP-1 Synergy/CompetitionGBS offers procedural alternative to semaglutide/tirzepatide for patients seeking durable non-pharmacological solution
Innovative Device PremiumClass III designation enables NRDL negotiation priority and hospital procurement preference under China’s medical device localization policy

Pipeline & Comprehensive Cycle Management

Strategic FocusExecution Plan
GBS CommercializationScale manufacturing; train endoscopists in tier-1/2 hospitals; establish reimbursement pathway
Product Line ExpansionAdjunctive devices for stent management, metabolic monitoring, and patient compliance
Digital Health IntegrationComprehensive cycle management platform combining device data with lifestyle coaching
Global ExpansionCE Mark and FDA regulatory pathway initiation post-HK listing

Competitive Landscape

CompetitorProductStatusTangji Differentiation
ValenTxEndoscopic bypass sleeve (US/EU)CE Mark; not in ChinaGBS first-mover China advantage; tailored to Asian anatomy
EndoBarrierDuodenal-jejunal bypass linerLimited commercial tractionGBS mimics RYGB more closely; superior metabolic outcomes
GI DynamicsEndoBarrier variantFinancial distressTangji stronger balance sheet post-IPO; NMPA regulatory credibility

Forward‑Looking Statements
This brief contains forward‑looking statements regarding Tangji Medtech’s Hong Kong IPO pricing and timing, GBS commercial adoption in Chinese hospitals, and endoscopic bariatric device market expansion. Actual results may differ due to HKEX listing approval delays, reimbursement negotiation outcomes with NMPA/NRDL, and competitive entry from global device manufacturers.-Fineline Info & Tech