Future Technology Co.,Ltd
China CN-MF-000049991 Last updated 8 Jun 2026
- Devices
- 264
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Prosthetic Parts Ref 4RC83T
Prosthetic Parts Ref 4R73T
Prosthetic Parts Ref 6R18
Prosthetic Parts Ref 4R44
Prosthetic Parts Ref 99B10
Prosthetic Parts Ref 1FC2
Prosthetic Parts Ref 3R21
Prosthetic Parts Ref 4R41S
Prosthetic Parts Ref 4R112
Prosthetic Parts Ref 1FC150
Prosthetic Parts Ref CHS70L-M
Prosthetic Parts Ref 4R44S
Prosthetic Parts Ref 4RC60S
Prosthetic Parts Ref HS200
Prosthetic Parts Ref 1FC350
Prosthetic Parts Ref HW30S
Prosthetic Parts Ref 2SR500
Prosthetic Parts Ref 1FC600
Prosthetic Parts Ref 1N04B
Prosthetic Parts Ref 4RC60A
Prosthetic Parts Ref 1FC500
Prosthetic Parts Ref 1NA1
Prosthetic Parts Ref 7E4A
Prosthetic Parts Ref 743A15
Prosthetic Parts Ref 1M10
Prosthetic Parts Ref SLP98
Prosthetic Parts Ref 4R42S
Prosthetic Parts Ref 4R74T
Prosthetic Parts Ref 3R22T
Prosthetic Parts Ref 3RC313D
Prosthetic Parts Ref 4R98T
Prosthetic Parts Ref 4RC61
Prosthetic Parts Ref CHS70R-S
Prosthetic Parts Ref 17PK
Prosthetic Parts Ref 1FC180
Prosthetic Parts Ref 1FC90
Prosthetic Parts Ref 3R17
Prosthetic Parts Ref 4R123
Prosthetic Parts Ref 42PPS
Prosthetic Parts Ref 3RC313DM
Prosthetic Parts Ref 2SR480
Prosthetic Parts Ref 6BS40
Prosthetic Parts Ref 4R122S
Prosthetic Parts Ref 1FC140
Prosthetic Parts Ref 4R41T
Prosthetic Parts Ref 3R22S
Prosthetic Parts Ref 4RC110
Prosthetic Parts Ref 4RC67A
Prosthetic Parts Ref 43SRC
Prosthetic Parts Ref 4R89S
Showing 101-150 of 264
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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