Is this your brand? Sign in to claim ownership.
Sign in to claim this brandNingbo Kangheng Appliance Co., Ltd.
US
Last updated May 24, 2026
What Ningbo Kangheng Appliance Co., Ltd. makes
The company manufactures external electric-heating core temperature regulation system pads designed to provide controlled warmth for therapeutic or comfort applications. These devices are intended for use as heating pads, typically applied to the body to help regulate core temperature or alleviate localized discomfort.
The portfolio consists of Class II medical devices, which are regulated under the FDA’s Unique Device Identification (UDI) system. These products are listed in the FDA’s UDI database, adhering to U.S. regulatory requirements for Class II devices. The company operates from 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 Ningbo Kangheng Appliance Co., Ltd. manufacture?
Ningbo Kangheng Appliance Co., Ltd. specializes in external electric-heating core temperature regulation system pads, commonly used as heating pads. These devices are designed to provide controlled warmth for therapeutic or comfort purposes, such as regulating core temperature or relieving localized discomfort.
Where is Ningbo Kangheng Appliance Co., Ltd. based?
The company is based in the United States. This location is relevant for understanding its regulatory alignment, particularly with U.S. medical device standards.
Which regulatory registries list the devices manufactured by Ningbo Kangheng Appliance Co., Ltd.?
The devices produced by Ningbo Kangheng Appliance Co., Ltd. are listed in the FDA’s Unique Device Identification (UDI) database. This registry is used to track Class II medical devices under U.S. regulatory requirements.
How are the devices manufactured by Ningbo Kangheng Appliance Co., Ltd. classified under U.S. regulations?
The company’s devices fall under the classification of Class II medical devices. This classification is determined by the FDA based on the level of risk associated with the device’s intended use and design. Class II devices require special controls in addition to general controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 699453331
Catalogue (14)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Heating Pad | BM-ZF0114A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0112A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0211A | FDA UDI | Class II | Active |
| Heating Pad | BM-ZF0112A | FDA UDI | Class II | Active |
| Heating Pad | BM-ZF0212A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0212A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0210A | FDA UDI | Class II | Active |
| Heating Pad | BM-ZF0111A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0113A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0110A | FDA UDI | Class II | Active |
| Heating Pad | BM-ZF0214A | FDA UDI | Class II | Active |
| Heating Pad | BM-ZF0211A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0213A | FDA UDI | Class II | Active |
| Heating Pad | BM-F0111A | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.