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Suzhou Endophix Co., Ltd.

ChinaFDA applicant, unverified FDA FEI 3030514683

Devices
145
Registrations
FDA
FDA recalls
0

What Suzhou Endophix Co., Ltd. makes

Suzhou Endophix Co., Ltd. manufactures orthopedic fixation devices, including the Megaloop Button System for bone stabilization and a range of suture anchors for tendon and ligament repair. Their product line includes PEEK interference screws and sheaths for soft tissue attachment, as well as titanium suture anchors for joint and tendon reattachment procedures.

The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway. Their products are listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Company details

FDA FEI number
3030514683
DUNS number
620899345
Address
Room 202, Factory No.3, Lane 151, Fengli Road, SIP, 215000 Suzhou, Jiangsu Province, P.R. CHINA, Suzhou Jiangsu