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Double Medical Technology, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252729Universal Spinal SystemNovember 18, 2025
K242348Locking Screw,CoCrMoDecember 4, 2024
K233078Posterior Cervical Spine SystemNovember 22, 2023
K223753Cervical Plate SystemMarch 14, 2023
K221150Advanced Bone PlateJanuary 25, 2023
K221088Anatomic Bone PlateJanuary 18, 2023
K221090Metal Cannulated ScrewJanuary 10, 2023
K221221Advanced Intramedullary Nail SystemDecember 21, 2022
K220921Metal Bone ScrewDecember 12, 2022
K172830Double Medical Femoral Nail SystemAugust 24, 2018
K172828Double Medical Cage SystemFebruary 1, 2018
K151458Double Medical Universal Spine SystemAugust 22, 2016