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Tdm Co., Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K241128TDM Plate and Screw SystemDecember 5, 2024
K230071Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus InAugust 22, 2024
K240423TDM Anterior Cervical Plate SystemApril 8, 2024
K232115TDM Large Bone Plate and Screw SystemApril 5, 2024
K231860TDM Screw SystemJanuary 18, 2024
K221844TDM Lumbar Interbody Fusion Cage SystemAugust 17, 2022
K220285PINE Pedicle Screw SystemMay 19, 2022
K191057Park's Pectus SystemMarch 19, 2020
K190391TDM Plate and Screw SystemsNovember 15, 2019
K190830TDM Screw SystemsSeptember 13, 2019
K171808TDM Plate and Screw SystemMarch 15, 2018