In February 2025, Shanghai Microport Medbot(Group)Co.,Ltd.'s intraperitoneal endoscopic single-port surgical system was approved for medical device registration (NMPA) with model SA-1000. This is the only single-port surgical robot in China and the second globally with a kinematic fixed point as of the registration date, making it the third single-port laparoscopic robot in China following SURGERII and Edge®.
In April 2025, the Capsule Endoscopy System registered by Chongqing Jinshan Sciences & Technology Group Co., Ltd. was approved for medical device registration (NMPA) with model number CC100, becoming the first dual-camera small intestine endoscope in China.
In April 2025, Zhuhai Seesheen Medical Technology Co., Ltd received approval from the National Equities Exchange and Quotations (NEEQ) for listing. This coincided with the company's 11th anniversary in May.
In June 2025, the electronic endoscope image processor AQ-400 series registered by Shanghai Aohua Photoelectricity Endoscope Co.,Ltd. was approved for medical device registration certificate (NMPA), marking the first domestically produced 3D ultra-high definition flexible endoscope platform.
In July 2025, centralized procurement of endoscopes (gastrointestinal endoscopes and laparoscopes) was conducted in Jiangsu, Anhui, and other regions. The transaction prices were significantly lower than the daily procurement prices. White light and fluorescence laparoscopes were priced below 300,000 yuan limit for centralized procurement, while gastrointestinal endoscopes were priced at tens of thousands, hundreds of thousands, and hundreds of thousands of yuan. In December, centralized procurement of laparoscopes in Xiamen set new lows (see original article).
In July 2025, CITIC Securities Co., Ltd. released the Ninth Progress Report on the Initial Public Offering and Listing Guidance Work of Guangdong OptoMedic Technologies, Inc.
In August 2025, the sixth batch of national centralized procurement of high-value medical consumables was officially launched. For the first time, urological interventional consumables were included in the national procurement scope. Disposable ureteroscopes (catheters) were included in the centralized procurement scope, making them the first disposable endoscope to be procured through centralized procurement.
In August 2025, KARL STORZ Endoskope (Shanghai) Co., Ltd. received domestic medical device registration certificates (NMPA) for its medical endoscope cold light source and insufflator. This signifies that its main laparoscopic components, except for the lens, have all obtained domestic registration certificates.
In September 2025, the General Office of the State Council issued the "Notice on Implementing Domestic Product Standards and Related Policies in Government Procurement," which will take effect on January 1, 2026. The notice stipulates that the cost of components manufactured in China must reach a specified proportion under domestic product standards, with a transition period of 3-5 years.
In October 2025, the disposable malleable intracranial electronic endoscope catheter registered by RONEKI (Dalian) was approved for medical device registration certificate (NMPA). It is the world's first portable malleable neuroendoscopy, which solves the blind spots that traditional rigid endoscopes cannot reach.
In November 2025, Olympus (Suzhou) Medical Devices Co., Ltd.'s CV-1500-C image processing device received its National Medical Device Registration Certificate (NMPA), becoming the first 4K flexible endoscope main unit in China. Previously, earlier this year, its GIF-EZ1500-C upper gastrointestinal endoscope, surgical main unit OTV-S700-C, and light source CLL-S700-C also received their National Medical Device Registration Certificates (NMPA).
In December 2025, Johnson & Johnson Medical's Monarch Platform electronic bronchial endoscopy navigation control system completed its first installation at the General Hospital of the Chinese People's Liberation Army (301 Hospital). In September 2024, Intuitive Surgical's LON bronchial navigation operation control system was first installed at Shanghai Chest Hospital.
In December 2025, the EP-8000 electronic endoscope processor registered by Suzhou Fujifilm Imaging Equipment Co., Ltd. received the National Medical Device Registration Certificate (NMPA). The EP-8000 is a 4K main unit and is Fujifilm's third domestically produced main unit in China.
In December 2025, Shanghai Aohua Photoelectricity Endoscope Co.,Ltd. (Aohua Endoscopy) announced the completion of the first batch of human scientific research clinical trials of the ERCP surgical robot system at Nanjing University Medical School Affiliated Gulou Hospital. The robot was independently developed by Aohua Endoscopy and is the world's first robot used for human experiments. It is expected to be launched in 2027-2028.
In December 2025, Smith & Nephew, a leading orthopedic company, received NMPA approval for its import licenses for head, chest, and laparoscopic endoscopes and arthroscopic lenses.
As of December 2025, approximately 804 domestically produced endoscope main units have been successfully registered in China, of which approximately 174 were registered in 2025.
As of December 2025, approximately 285 disposable electronic endoscopes have been successfully registered in China, an increase of about 23 from the 262 registered in June. About 66 endoscopes were successfully registered in 2025, including the first appearance of disposable electronic spinal endoscopes and disposable electronic thoracic endoscopes. Registration of disposable ureteral and bronchial endoscopes has slowed, while bladder and uterine endoscopes have accelerated, and disposable gastrointestinal endoscopes have encountered some issues.
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We, Jiangxi Zhuoruihua Medical Instrument Co.,Ltd., is a manufacturer in China specializing in the endoscopic consumables, include GI line such as biopsy forceps, hemoclip, polyp snare, sclerotherapy needle, spray catheter, cytology brushes, guidewire, stone retrieval basket, nasal biliary drainage cathete etc. which are widely used in EMR, ESD, ERCP. And Urology Line, such as ureteral access sheath and ureteral access sheath with suction, disposable Urinary Stone Retrieval Basket, and urology guidewire etc.
Our products are CE certified, and our plants are ISO certified. Our goods have been exported to Europe, North America, Middle East and part of Asia, and widely obtains the customer of the recognition and praise!
Post time: Dec-19-2025