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Sign in to claim this brandWhat Double Medical Technology Inc. makes
Double Medical Technology Inc. manufactures orthopaedic fixation devices including non-bioabsorbable plates, bone screws, and internal fixation systems combining plates and screws. Their product range also includes tibia intramedullary nails, pin-sleeve bone screws, surgical implant handling forceps, and reusable orthopaedic implantation sleeves.
The company's devices are classified as Class II medical devices and are listed in the FDA's Unique Device Identification (fda_udi) system. Double Medical Technology Inc. is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What medical devices does Double Medical Technology Inc. manufacture?
Double Medical Technology Inc. manufactures orthopaedic fixation devices including non-bioabsorbable plates, bone screws, and internal fixation systems combining plates and screws. Their product range also includes tibia intramedullary nails, pin-sleeve bone screws, surgical implant handling forceps, and reusable orthopaedic implantation sleeves.
Where is Double Medical Technology Inc. based?
Double Medical Technology Inc. is based in the United States, as indicated by the country information provided in the device data.
Which regulatory registries list Double Medical Technology Inc.'s devices?
Double Medical Technology Inc.'s devices are listed in the FDA's Unique Device Identification (fda_udi) system, as specified in the device data.
How are Double Medical Technology Inc.'s devices classified?
Double Medical Technology Inc.'s devices are classified as Class II medical devices, which means they are subject to special controls to ensure their safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- double-medical.com
- —
- —
- [email protected]
- Phone
- +865926087101
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 529366055
Catalogue (1729)
Page 28 of 35| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| 6.5mm Cancellous Screw, Fully Threaded | 040060040 | FDA UDI | Class II | Active |
| 2.4mm Locking Screw | 040670012 | FDA UDI | Class II | Active |
| L-Buttress Locking Plate | 020162004 | FDA UDI | Class II | Active |
| Fixation Sleeve, φ3.4 | 111226000 | FDA UDI | Class II | Active |
| Bending Iron, Left | 110070500 | FDA UDI | Class II | Active |
| 3.5mm Locking Screw, Self-drilling | 040080014 | FDA UDI | Class II | Active |
| Lateral Tibial Head Buttress Locking Plate Ⅰ | 020271008 | FDA UDI | Class II | Active |
| Distal Medial Tibial Locking Plate III | 021491010 | FDA UDI | Class II | Active |
| 2.7S-Mini Screw | 030210009 | FDA UDI | Class II | Active |
| Slide Hammer | 111193200 | FDA UDI | Class II | Active |
| Distal Fibular Locking Plate | 020201009 | FDA UDI | Class II | Active |
| Distal Medial Tibial Locking Plate | 020182007 | FDA UDI | Class II | Active |
| Wrench for Fixation Sleeve | 110201800 | FDA UDI | Class II | Active |
| Torque Indicating Screwdriver, 4.0 N-m | 110070700 | FDA UDI | Class II | Active |
| Distal Medial Tibial Locking Plate, Combi-holes | 020452009 | FDA UDI | Class II | Active |
| Distal Humeral Sub-Condylar Locking Plate, Combi-holes | 020621004 | FDA UDI | Class II | Active |
| 4.5mm Cortex Screw | 040040060 | FDA UDI | Class II | Active |
| Distal Lateral Tibial Locking Plate, Combi-holes | 020461012 | FDA UDI | Class II | Active |
| Lateral Tibial Head Buttress Locking Plate I, Combi-holes | 020442003 | FDA UDI | Class II | Active |
| Small Limited Contact Locking Plate, Combi-holes | 020470003 | FDA UDI | Class II | Active |
| 3.5mm Cortex Screw | 040010075 | FDA UDI | Class II | Active |
| 3.5mm Cortex Screw | 040010024 | FDA UDI | Class II | Active |
| 3.0mm Heberden Screw | 060010036 | FDA UDI | Class II | Active |
| 5.0mm Locking screw, Self-tapping | 040090018 | FDA UDI | Class II | Active |
| 2.7S-Mini Locking Screw | 030340019 | FDA UDI | Class II | Active |
| Proximal Femoral Locking Plate, Combi-holes | 020421006 | FDA UDI | Class II | Active |
| Lateral Tibial Head Buttress Locking Plate II | 021361006 | FDA UDI | Class II | Active |
| Distal Femoral Locking Plate II | 021352015 | FDA UDI | Class II | Active |
| 5.0mm Locking screw, Self-tapping | 040090080 | FDA UDI | Class II | Active |
| Broad Limited Contact Locking Plate | 020120015 | FDA UDI | Class II | Active |
| 6.5mm Cancellous Screw, Half Threaded | 040050035 | FDA UDI | Class II | Active |
| 7.3mm Non-locking Screw, Half Threaded | 040110070 | FDA UDI | Class II | Active |
| Lateral Tibial Head Buttress Locking Plate I, Combi-holes | 020441008 | FDA UDI | Class II | Active |
| Proximal Femoral Locking Plate | 020241004 | FDA UDI | Class II | Active |
| 4.5mm Cortex Screw | 040040042 | FDA UDI | Class II | Active |
| 7.3mm Non-locking Screw, Fully Threaded | 040120075 | FDA UDI | Class II | Active |
| Reconstruction Locking Plate | 020290013 | FDA UDI | Class II | Active |
| Double Drill Guide, φ2.5/φ3.5 | 110041100 | FDA UDI | Class II | Active |
| Universal Tibial Nail, Cannulated | 070010255 | FDA UDI | Class II | Active |
| Distal Femoral Locking Plate Ⅱ, Combi-holes | 021431006 | FDA UDI | Class II | Active |
| 1.5S-Mini Screw | 030070019 | FDA UDI | Class II | Active |
| Olecranon Locking Plates Ⅲ, Combi-holes | 020520004 | FDA UDI | Class II | Active |
| Distal Medial Tibial Locking Plate II | 021502010 | FDA UDI | Class II | Active |
| Bone Lever, Large | 110072400 | FDA UDI | Class II | Active |
| Aiming Arm for UTN | 110300200 | FDA UDI | Class II | Active |
| Drill Bit, φ3.4, length 280mm | 111225900 | FDA UDI | Class II | Active |
| SW 2.5 Hexagonal Screwdriver Shaft | 110023300 | FDA UDI | Class II | Active |
| Connecting Screw, for insertion handle | 111222700 | FDA UDI | Class II | Active |
| Tissue Protector | 111220600 | FDA UDI | Class II | Active |
| Double Claw Reduction Forceps | 110020800 | FDA UDI | Class II | Active |
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