Tdm Co., Ltd. is one of 440 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Tdm Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: TDM Large Bone Plate and Screw System, NOVIX Pedicle Screw System, TDM Plate and Screw System
13
Total
13
Cleared
0
Denied
Tdm Co., Ltd. has 13 FDA 510(k) cleared orthopedic devices. Based in Gwangju, KR.
Latest FDA clearance: Oct 2026. Active since 2018.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Eerkie Corporation, Lince Consulting, LLC and Dave Kim.
FDA 510(k) Regulatory Record - Tdm Co., Ltd.
13 devices
Cleared
Oct 02, 2026
TDM Large Bone Plate and Screw System
Orthopedic
140d
Cleared
Oct 01, 2026
NOVIX Pedicle Screw System
Orthopedic
30d
Cleared
Dec 05, 2024
TDM Plate and Screw System
Orthopedic
225d
Cleared
Aug 22, 2024
Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking...
Orthopedic
590d
Cleared
Apr 08, 2024
TDM Anterior Cervical Plate System
Orthopedic
55d
Cleared
Apr 05, 2024
TDM Large Bone Plate and Screw System
Orthopedic
266d
Cleared
Jan 18, 2024
TDM Screw System
Orthopedic
209d
Cleared
Aug 17, 2022
TDM Lumbar Interbody Fusion Cage System
Orthopedic
54d
Cleared
May 19, 2022
PINE Pedicle Screw System
Orthopedic
107d
Cleared
Mar 19, 2020
Park's Pectus System
Orthopedic
332d
Cleared
Nov 15, 2019
TDM Plate and Screw Systems
Orthopedic
269d
Cleared
Sep 13, 2019
TDM Screw Systems
Orthopedic
165d