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Sign in to claim this brandShenzhen Jian Feng Electronic Technology Co., Ltd.
US
Last updated May 24, 2026
What Shenzhen Jian Feng Electronic Technology Co., Ltd. makes
Shenzhen Jian Feng Electronic Technology Co., Ltd. manufactures physical therapy transcutaneous neuromuscular electrical stimulation (TENS/NMES) systems designed for muscle stimulation and pain management. These devices deliver controlled electrical impulses through electrodes applied to the skin to target specific muscle groups or nerve pathways, commonly used in rehabilitation and therapeutic settings.
The company’s portfolio is regulated under Class II medical devices in the US, with products authorised via the FDA’s 510(k) premarket notification process and listed under the Unique Device Identifier (UDI) system. The manufacturer operates from the United States, adhering to applicable regulatory requirements for these therapeutic electrical stimulation devices.
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 Shenzhen Jian Feng Electronic Technology Co., Ltd. primarily manufacture?
Shenzhen Jian Feng Electronic Technology Co., Ltd. specialises in physical therapy transcutaneous neuromuscular electrical stimulation (TENS/NMES) systems. These devices are designed to deliver controlled electrical impulses through electrodes placed on the skin, targeting muscle stimulation or nerve pathways for therapeutic purposes. They are commonly used in rehabilitation and pain management settings.
Where is Shenzhen Jian Feng Electronic Technology Co., Ltd. based, and how does this affect its regulatory compliance?
The company is based in the United States, which means its devices must comply with US FDA regulations. Since its products fall under Class II classification, they undergo 510(k) premarket notification for authorisation and are tracked via the FDA’s Unique Device Identifier (UDI) system. This ensures transparency and adherence to safety standards for therapeutic electrical stimulation devices.
Which regulatory registries or databases list Shenzhen Jian Feng Electronic Technology Co., Ltd.’s devices?
The company’s devices are authorised through the FDA’s 510(k) process and are listed under the Unique Device Identifier (UDI) system. These registries ensure traceability and compliance tracking for Class II medical devices, including TENS/NMES systems, in the US market.
How are Shenzhen Jian Feng Electronic Technology Co., Ltd.’s devices classified under US regulations?
The company’s physical therapy TENS/NMES systems are classified as Class II medical devices in the US. This classification requires premarket notification (510(k)) to demonstrate substantial equivalence to a legally marketed predicate device, ensuring they meet safety and performance standards before authorisation.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- avcoo.com
- —
- —
- [email protected]
- Phone
- +1(678)829-7251
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 560082555
Catalogue (46)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Belifu | FM-B2403 | FDA UDI | Class II | Active |
| No | FM-B2403A | FDA UDI | Class II | Active |
| No | FM-B2405 | FDA UDI | Class II | Active |
| No | AS8016 | FDA UDI | Class II | Active |
| No | TU3424 | FDA UDI | Class II | Active |
| No | FM-B2404 | FDA UDI | Class II | Active |
| No | TA3224 | FDA UDI | Class II | Active |
| No | FM-B1501A | FDA UDI | Class II | Active |
| No | FM-B2409 | FDA UDI | Class II | Active |
| No | AS1080 | FDA UDI | Class II | Active |
| No | TP2208 | FDA UDI | Class II | Active |
| No | TU1130 | FDA UDI | Class II | Active |
| No | FM-B2404 | FDA UDI | Class II | Active |
| No | TU2224 | FDA UDI | Class II | Active |
| No | TA2224C | FDA UDI | Class II | Active |
| No | TA2224 | FDA UDI | Class II | Active |
| No | AS8012 | FDA UDI | Class II | Active |
| No | AS8012 | FDA UDI | Class II | Active |
| No | FM-B2402 | FDA UDI | Class II | Active |
| Auvon | TA2224C | FDA UDI | Class II | Active |
| No | AS8016 | FDA UDI | Class II | Active |
| Avcoo | TA2224C | FDA UDI | Class II | Active |
| No | TUP324 | FDA UDI | Class II | Active |
| No | AS9020 | FDA UDI | Class II | Active |
| No | AS8019 | FDA UDI | Class II | Active |
| No | AS8016 | FDA UDI | Class II | Active |
| No | AS8012 | FDA UDI | Class II | Active |
| No | YK15AB | FDA UDI | Class II | Active |
| No | FM-B2406 | FDA UDI | Class II | Active |
| No | AS9020 | FDA UDI | Class II | Active |
| No | TA3224 | FDA UDI | Class II | Active |
| No | TA2224 | FDA UDI | Class II | Active |
| No | AS9020 | FDA UDI | Class II | Active |
| No | FM-B2409 | FDA UDI | Class II | Active |
| No | AS9020 | FDA UDI | Class II | Active |
| No | AS8016 | FDA UDI | Class II | Active |
| No | AS8019 | FDA UDI | Class II | Active |
| No | TU1130 | FDA UDI | Class II | Active |
| No | AS8012 | FDA UDI | Class II | Active |
| No | AS8012C | FDA UDI | Class II | Active |
| No | FM-B2407 | FDA UDI | Class II | Active |
| Avcoo | TU2424 | FDA UDI | Class II | Active |
| TENS & EMS DEVICE (Model: FM-B2403A) | K213741 | FDA 510(k) | Class II | Active |
| TENS & EMS Device | K202866 | FDA 510(k) | Class II | Active |
| TENS & EMS Device | K213835 | FDA 510(k) | Class II | Active |
| Tens & Ems Device | K223825 | FDA 510(k) | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
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Notified Bodies
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Authorities
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Shenzhen Jian Feng Electronic Technology Co., Ltd Shenzhen Guangdong · CN FEI 3009488655