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Sign in to claim this brandChangzhou Langcheng Intelligence Technology Co., Ltd.
US
Last updated May 25, 2026
What Changzhou Langcheng Intelligence Technology Co., Ltd. makes
The company manufactures foldable walking chairs designed for mobility assistance, including models such as LANCN, LCJ, and LCJ. These devices are intended for temporary or portable use to aid individuals with limited mobility in indoor or outdoor environments.
The walking chairs fall under Class I regulatory classification and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable domestic regulatory requirements for these products.
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 Changzhou Langcheng Intelligence Technology Co., Ltd. manufacture?
The company specializes in foldable walking chairs, which are designed to assist individuals with limited mobility. These devices are intended for temporary or portable use in both indoor and outdoor settings, providing support for safe movement.
Where is Changzhou Langcheng Intelligence Technology Co., Ltd. based?
The company is based in the United States, where it operates and develops its foldable walking chair products. Its location ensures compliance with U.S. regulatory requirements for these mobility assistance devices.
How are the devices manufactured by Changzhou Langcheng Intelligence Technology Co., Ltd. classified under regulatory standards?
The foldable walking chairs produced by the company fall under Class I regulatory classification. This classification is typically assigned to low-risk medical devices, such as mobility aids, where the risk of harm is minimal and general controls are sufficient for ensuring safety and effectiveness.
Are the devices manufactured by Changzhou Langcheng Intelligence Technology Co., Ltd. listed in any regulatory databases?
Yes, the company’s foldable walking chairs are included in the FDA’s Unique Device Identifier (UDI) database. Listing in this registry helps ensure traceability and transparency in the supply chain, which is important for regulatory oversight and patient safety.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 711845159
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