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Sign in to claim this brandSichuan Qianli-Beoka Medical Technology, Inc.
US
Last updated May 23, 2026
What Sichuan Qianli-Beoka Medical Technology, Inc. makes
The company manufactures wearable electric massagers designed for muscle relaxation and pain relief, including multiple iterations of the BEOKA device.
These devices are classified as Class II under FDA regulations and are authorised via 510(k) and UDI listings 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 Sichuan Qianli-Beoka Medical Technology, Inc. manufacture?
Sichuan Qianli-Beoka Medical Technology, Inc. specializes in wearable electric massagers. These devices are primarily designed for muscle relaxation and pain relief, targeting consumer and therapeutic markets where non-invasive muscle stimulation is sought. The company’s portfolio includes multiple iterations of its flagship product, the BEOKA.
Where is Sichuan Qianli-Beoka Medical Technology, Inc. based?
The company is based in the United States. While the specific location isn’t detailed, its regulatory filings and device listings are submitted through the U.S. system, indicating its primary operational or legal presence is within the country.
Which regulatory registries list devices manufactured by Sichuan Qianli-Beoka Medical Technology, Inc.?
Devices from Sichuan Qianli-Beoka Medical Technology, Inc. are listed in the FDA’s 510(k) premarket notification database and the FDA’s Unique Device Identifier (UDI) system. These registries confirm the devices’ authorised status under U.S. regulations, where Class II classification applies.
How are devices from Sichuan Qianli-Beoka Medical Technology, Inc. classified under FDA regulations?
All devices manufactured by Sichuan Qianli-Beoka Medical Technology, Inc. fall under Class II classification by the FDA. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as wearable electric massagers. The classification is determined based on the device’s intended use and potential risks.
AI-generated from registry data and not verified by a human reviewer.
Information
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- US
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Catalogue (14)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Beoka | ACM-A2/Beoka/Black(XL)/Standard Edition | FDA UDI | Class II | Active |
| Beoka | ACM-A1/Black M (Luxury version) | FDA UDI | Class II | Active |
| Beoka | ACM-A2/Beoka/Black(M)/Standard Edition | FDA UDI | Class II | Active |
| Beoka | ACM-A1/Black S (Luxury version) | FDA UDI | Class II | Active |
| Beoka | ACM-A1/Beoka/Black(M)/Standard Edition | FDA UDI | Class II | Active |
| Beoka | ACM-PLUS-A2/Black L/Luxury version | FDA UDI | Class II | Active |
| Beoka | ACM-PLUS-A2/Black M/Luxury version | FDA UDI | Class II | Active |
| Beoka | ACM-A1/Beoka/Black(XL)/Standard Edition | FDA UDI | Class II | Active |
| Beoka | ACM-A1/Beoka/Black(S)/Standard Edition | FDA UDI | Class II | Active |
| Beoka | ACM-A2/Beoka/Black(L)/Standard Edition | FDA UDI | Class II | Active |
| Beoka | ACM-A1/Black L (Luxury version) | FDA UDI | Class II | Active |
| Beoka | ACM-A1/Beoka/Black(L)/Standard Edition | FDA UDI | Class II | Active |
| Beoka | ACM-A2/Beoka/Black(S)/Standard Edition | FDA UDI | Class II | Active |
| Air compression massager (ACM-PLUS-A1, ACM-PLUS-A2, ACM-PLUS-A3, ACM-PLUS-A4, ACM-PLUS-A5, ACM-PLUS-A6) | K243206 | 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.
- Sichuan Qianli-Beoka Medical Technology Inc. Chengdu Sichuan · CN FEI 3018455773