Future Technology Co.,Ltd
China CN-MF-000049991 Last updated 8 Jun 2026
- Devices
- 264
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Prosthetic Parts Ref 4R72A
Prosthetic Parts Ref 4R47
Prosthetic Parts Ref 1FA2
Prosthetic Parts Ref HS70-SCM
Prosthetic Parts Ref 4RC255S=22
Prosthetic Parts Ref 716Y4
Prosthetic Parts Ref 1FC10
Prosthetic Parts Ref 99B26
Prosthetic Parts Ref 15WJA
Prosthetic Parts Ref 6R23
Prosthetic Parts Ref 3R40A
Prosthetic Parts Ref 40BFS
Prosthetic Parts Ref 1FS
Prosthetic Parts Ref 4R77S
Prosthetic Parts Ref 6R16
Prosthetic Parts Ref 45SCR
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Authorised representatives
What Future Technology Co.,Ltd makes
Future Technology Co., Ltd. specialises in prosthetic parts, including components designed for lower-limb and upper-limb prosthetics. These devices are intended to restore mobility and functionality for users requiring limb replacement solutions.
The company’s prosthetic parts are classified as Class I medical devices and are registered in the EU’s eudamed database. The portfolio is primarily regulated under EU Medical Device Regulations, with listings maintained in the official EU device registry.
Frequently asked questions
What types of medical devices does Future Technology Co., Ltd. manufacture?
Future Technology Co., Ltd. specialises in prosthetic parts, specifically components for lower-limb and upper-limb prosthetics. These devices are designed to help users regain mobility and functionality after limb loss or amputation.
Where is Future Technology Co., Ltd. based?
Future Technology Co., Ltd. is based in China (CN). The company’s prosthetic parts are developed and manufactured there, adhering to relevant regulatory standards.
Which regulatory registries list Future Technology Co., Ltd.’s devices?
Future Technology Co., Ltd.’s prosthetic parts are listed in the eudamed database, the official EU registry for medical devices. This registry ensures transparency and traceability of devices authorised under EU Medical Device Regulations.
How are Future Technology Co., Ltd.’s prosthetic parts classified under medical device regulations?
Future Technology Co., Ltd.’s prosthetic parts fall under Class I classification in the EU’s medical device framework. This classification applies due to their low-risk profile, as they are primarily mechanical components intended for limb replacement without significant biological interaction.
Are Future Technology Co., Ltd.’s devices regulated under EU Medical Device Regulations?
Yes, Future Technology Co., Ltd.’s prosthetic parts are regulated under the EU Medical Device Regulations (MDR) when marketed in the European Union. The company maintains listings in eudamed to comply with these requirements, ensuring transparency and regulatory alignment.
Information
- Country
- China
- Address
- 930,S10, Huarun Zhidi,#52 Hongshanyuan Road,Gulou District, , Fuzhou City, Fujian Province, China
- Website
- futureonp.com
- [email protected]
- PRRC contact
- Xiaoyang Lin
- EUDAMED SRN
- CN-MF-000049991