Double Medical Technology, Inc.
Double Medical Technology, Inc. appears in FDA public data with 0 recalls, 12 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Nov 18, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 12
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K252729 | Universal Spinal System | Nov 18, 2025 |
| K242348 | Locking Screw,CoCrMo | Dec 4, 2024 |
| K233078 | Posterior Cervical Spine System | Nov 22, 2023 |
| K223753 | Cervical Plate System | Mar 14, 2023 |
| K221150 | Advanced Bone Plate | Jan 25, 2023 |
| K221088 | Anatomic Bone Plate | Jan 18, 2023 |
| K221090 | Metal Cannulated Screw | Jan 10, 2023 |
| K221221 | Advanced Intramedullary Nail System | Dec 21, 2022 |
| K220921 | Metal Bone Screw | Dec 12, 2022 |
| K172830 | Double Medical Femoral Nail System | Aug 24, 2018 |
| K172828 | Double Medical Cage System | Feb 1, 2018 |
| K151458 | Double Medical Universal Spine System | Aug 22, 2016 |