Double Medical Technology, Inc. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Double Medical Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Universal Spinal System, Locking Screw,CoCrMo, Posterior Cervical Spine System
12
Total
12
Cleared
0
Denied
Double Medical Technology, Inc. has 12 FDA 510(k) cleared orthopedic devices. Based in Xiamen, CN.
Latest FDA clearance: Nov 2025. Active since 2016.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Double Medical Technology, Inc.
12 devices
Cleared
Nov 18, 2025
Universal Spinal System
Orthopedic
82d
Cleared
Dec 04, 2024
Locking Screw,CoCrMo
Orthopedic
118d
Cleared
Nov 22, 2023
Posterior Cervical Spine System
Orthopedic
58d
Cleared
Mar 14, 2023
Cervical Plate System
Orthopedic
90d
Cleared
Jan 25, 2023
Advanced Bone Plate
Orthopedic
280d
Cleared
Jan 18, 2023
Anatomic Bone Plate
Orthopedic
280d
Cleared
Jan 10, 2023
Metal Cannulated Screw
Orthopedic
272d
Cleared
Dec 21, 2022
Advanced Intramedullary Nail System
Orthopedic
238d
Cleared
Dec 12, 2022
Metal Bone Screw
Orthopedic
257d
Cleared
Aug 24, 2018
Double Medical Femoral Nail System
Orthopedic
340d
Cleared
Feb 01, 2018
Double Medical Cage System
Orthopedic
136d
Cleared
Aug 22, 2016
Double Medical Universal Spine System
Orthopedic
448d