Future Technology Co.,Ltd
China CN-MF-000049991 Last updated 8 Jun 2026
- Devices
- 264
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
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
Prosthetic Parts Ref 4R30A
Prosthetic Parts Ref 2R38S
Prosthetic Parts Ref 25PL
Prosthetic Parts Ref 2RC40T
Prosthetic Parts Ref 21V15
Prosthetic Parts Ref 2SR100
Prosthetic Parts Ref 2R3S
Prosthetic Parts Ref 2S1S-26-30
Prosthetic Parts Ref 21VH02
Prosthetic Parts Ref 2SR380
Prosthetic Parts Ref 2R14
Prosthetic Parts Ref 2N33
Prosthetic Parts Ref 4R157T-B
Prosthetic Parts Ref 2MA
Prosthetic Parts Ref 2R3A
Prosthetic Parts Ref 6R19
Prosthetic Parts Ref 4R105
Prosthetic Parts Ref 4R84A
Prosthetic Parts Ref 4R43
Prosthetic Parts Ref 3R21T
Prosthetic Parts Ref 36VBL
Prosthetic Parts Ref 1S24W
Prosthetic Parts Ref 4RC75T
Prosthetic Parts Ref 729F3
Prosthetic Parts Ref CHS80R
Prosthetic Parts Ref 6T2
Prosthetic Parts Ref 4R89
Prosthetic Parts Ref 37CMP
Prosthetic Parts Ref 21B37
Prosthetic Parts Ref 15DP
Prosthetic Parts Ref 4RC255S=30
Prosthetic Parts Ref 3R15T
Prosthetic Parts Ref 6BT50T-11
Prosthetic Parts Ref 1FK
Prosthetic Parts Ref HS32
Prosthetic Parts Ref 4R74S
Prosthetic Parts Ref 6BT50
Prosthetic Parts Ref 616S
Prosthetic Parts Ref 7E7
Prosthetic Parts Ref 4RC75
Prosthetic Parts Ref 4R42
Prosthetic Parts Ref 4RC117S
Prosthetic Parts Ref 4R6S
Prosthetic Parts Ref 4R57S
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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