Future Technology Co.,Ltd
China CN-MF-000049991 Last updated 8 Jun 2026
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- Devices
- 260
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Prosthetic Parts Ref 28MP30
Prosthetic Parts Ref 2R45
Prosthetic Parts Ref 2R12
Prosthetic Parts Ref 2R11
Prosthetic Parts Ref 2R3CT
Prosthetic Parts Ref 2R44
Prosthetic Parts Ref 21P20
Prosthetic Parts Ref 28MP2
Prosthetic Parts Ref 4R133T
Prosthetic Parts Ref 28MP
Prosthetic Parts Ref 4R22
Prosthetic Parts Ref 2RC41S=160
Prosthetic Parts Ref 4R38
Prosthetic Parts Ref 4R157S-A
Prosthetic Parts Ref 4R133S
Prosthetic Parts Ref 4R21S
Prosthetic Parts Ref 4R19T
Prosthetic Parts Ref 21PF
Prosthetic Parts Ref 4R136S
Prosthetic Parts Ref 2R2
Prosthetic Parts Ref 4R21A
Prosthetic Parts Ref 4R24
Prosthetic Parts Ref 4R131
Prosthetic Parts Ref 22CF
Prosthetic Parts Ref 2S2S-26-30
Prosthetic Parts Ref 4R202S
Prosthetic Parts Ref 2SR380AM
Prosthetic Parts Ref 21VR551
Prosthetic Parts Ref 4R123S
Prosthetic Parts Ref 4R202T
Prosthetic Parts Ref 2RC41
Prosthetic Parts Ref 4R19
Prosthetic Parts Ref 4R30T
Prosthetic Parts Ref 21VR552
Prosthetic Parts Ref 2R3
Prosthetic Parts Ref 2N33S
Prosthetic Parts Ref 4R20A
Prosthetic Parts Ref 21VS20
Prosthetic Parts Ref 29NL
Prosthetic Parts Ref 4R24A
Prosthetic Parts Ref 2R22
Prosthetic Parts Ref 2N1T
Prosthetic Parts Ref 2S1S-22-25
Prosthetic Parts Ref 23CF
Prosthetic Parts Ref 2R3T
Prosthetic Parts Ref 4R21T
Prosthetic Parts Ref 4R28
Prosthetic Parts Ref 4R24T
Prosthetic Parts Ref 2S1T-22-25
Prosthetic Parts Ref 28TH30
Showing 1-50 of 260
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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