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Sign in to claim this brandChongquin Jinshan Science & Technology (Group) Co., Ltd.
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Last updated May 23, 2026
What Chongquin Jinshan Science & Technology (Group) Co., Ltd. makes
Chongqin Jinshan Science & Technology (Group) Co., Ltd. manufactures hysteroscopy systems, which are endoscopic devices used for visual inspection and minimally invasive procedures within the uterine cavity.
The company’s hysteroscopy systems are classified as Class II medical devices under FDA regulations and are recorded in the 510(k) premarket notification process in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Chongqin Jinshan Science & Technology (Group) Co., Ltd. manufacture?
Chongqin Jinshan Science & Technology (Group) Co., Ltd. specializes in hysteroscopy systems, which are endoscopic devices designed for visual examination and minimally invasive procedures inside the uterine cavity. These systems are intended to assist healthcare professionals in diagnosing and treating conditions within the uterus.
Where is Chongqin Jinshan Science & Technology (Group) Co., Ltd. based?
The company is based in the United States. While the name suggests a Chinese origin, its operational headquarters and regulatory filings are conducted through its US entity.
How are the company’s hysteroscopy systems classified under medical device regulations?
The hysteroscopy systems manufactured by Chongqin Jinshan Science & Technology (Group) Co., Ltd. are classified as Class II medical devices under FDA regulations. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as sterility, labeling requirements, or performance standards.
Which regulatory registries or databases list the company’s devices?
The company’s hysteroscopy systems are recorded in the FDA’s 510(k) premarket notification process, meaning these devices have undergone review to demonstrate substantial equivalence to a legally marketed predicate device. This registry is part of the FDA’s database for Class II devices in the United States.
Why is the 510(k) process relevant for the company’s hysteroscopy systems?
The 510(k) process is a key regulatory pathway for Class II devices in the US, including hysteroscopy systems. It ensures that the company’s devices meet FDA requirements for safety and performance by demonstrating they are substantially equivalent to a previously cleared device (the
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (13)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Beamer Aveo Irrigation Pump Bottle Holder (us/Eu) Replacement Part | PUMP-3 | FDA UDI | Class II | Active |
| alpHaONE | JSPC-1 | FDA UDI | Class I | Active |
| Beamer AVEO™ Irrigation Pump | AVEOPUMP | FDA UDI | Class II | Unknown |
| Beamer Aveo Irrigation Pump Head Replacement Part | PUMP-2 | FDA UDI | Class II | Active |
| alpHaONE | JSPR-3 | FDA UDI | Class I | Active |
| GynoVision | JSX-T-8 | FDA UDI | Class II | Active |
| alpHaONE | JSPR-3 | FDA UDI | Class I | Active |
| Beamer Aveo Irrigation Pump Foot Pedal Replacement Part | PUMP-1 | FDA UDI | Class II | Unknown |
| GynoVision | JSX-T-7 | FDA UDI | Class II | Active |
| GynoVision | JSX-1 | FDA UDI | Class II | Active |
| alpHaONE | JSPC-1 | FDA UDI | Class I | Active |
| GynoVision | JSX-T-6 | FDA UDI | Class II | Active |
| Hysteroscopy System | K172151 | FDA 510(k) | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Chongqing Jinshan Science & Technology (group) Co., Ltd Chongqing · CN FEI 3011219572