Shanghai Sanyou Medical Co, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shanghai Sanyou Medical Co, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™ Direction Changeable Lumbar Cage System, KEYSTONE Cage System, Zeus Spinal System, Adena-Zina Spinal System
9
Total
9
Cleared
0
Denied
Shanghai Sanyou Medical Co, Ltd. has 9 FDA 510(k) cleared medical devices. Based in Bartlett, US.
Last cleared in 2023. Active since 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Shanghai Sanyou Medical Co, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Shanghai Sanyou Medical Co, Ltd.
9 devices
Cleared
Dec 12, 2023
Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™...
Orthopedic
257d
Cleared
Oct 10, 2023
Zeus Spinal System
Orthopedic
188d
Cleared
Jul 28, 2023
Adena-Zina Spinal System
Orthopedic
28d
Cleared
Sep 21, 2021
KEYSTONE PEEK Cage System
Orthopedic
111d
Cleared
Aug 16, 2021
Adena-Zina System
Orthopedic
45d
Cleared
Oct 05, 2017
Shanghai Sanyou CARMEN Cervical Fusion System
Orthopedic
309d
Cleared
Sep 18, 2017
Shanghai Sanyou PEEK Cage System
Orthopedic
286d
Cleared
Feb 12, 2016
Adena-Zina System
Orthopedic
140d
Cleared
Aug 07, 2013
KATIA SYSTEM
Orthopedic
71d