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Double Medical Technology Inc.

US

Last updated May 29, 2026

Part of Double Medical Technology Inc.

What 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
—
LinkedIn
—
Facebook
—
Phone
+865926087101
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
529366055

Catalogue (1729)

Page 35 of 35
DeviceModel / ReferenceRegistriesClassStatus
Clavicular Locking Plate 020032009
FDA UDI
Class IIActive
6.5mm Cancellous Screw, Fully Threaded 040060075
FDA UDI
Class IIActive
Distal Fibular Locking Plate, Combi-holes 020512003
FDA UDI
Class IIActive
3.0mm Heberden Screw 060010014
FDA UDI
Class IIActive
Distal Lateral Tibial Locking Plate 020191011
FDA UDI
Class IIActive
Clavicular Locking Plate, Combi-holes 020501010
FDA UDI
Class IIActive
Distal Lateral Tibial Locking Plate, Combi-holes 020462010
FDA UDI
Class IIActive
7.3mm Cannulated Screw, Short Threaded 060080090
FDA UDI
Class IIActive
4.5mm Cortex Screw 040040048
FDA UDI
Class IIActive
Distal Medial Tibial Locking Plate 020181003
FDA UDI
Class IIActive
Proximal Posterior Tibial Locking Plate 020691007
FDA UDI
Class IIActive
Distal Femoral Locking Plate I 020262008
FDA UDI
Class IIActive
3.5mm Locking Screw, Self-drilling 040080020
FDA UDI
Class IIActive
Lateral Tibial Head Buttress Locking Plate II, Combi-holes 021442003
FDA UDI
Class IIActive
T-Type Retracter 110021500
FDA UDI
Class IIActive
Proximal Femoral Locking Plate, Combi-holes 020422013
FDA UDI
Class IIActive
6.5mm Cancellous Screw, Half Threaded 040050055
FDA UDI
Class IIActive
Template (Curved) 110022100
FDA UDI
Class IIActive
5.0mm Dual Core Locking Screw 071260050
FDA UDI
Class IIActive
Lateral Tibial Head Buttress Locking Plate Ⅰ 020272010
FDA UDI
Class IIActive
6.5mm Cancellous Screw, Fully Threaded 040060085
FDA UDI
Class IIActive
2.7S-Mini Locking Screw 030340010
FDA UDI
Class IIActive
Bone Lever, Small 110042300
FDA UDI
Class IIActive
Connecting Screw, cannulated, short, for Tibial Nail 110300500
FDA UDI
Class IIActive
3.5mm Locking Screw, Self-drilling 040080060
FDA UDI
Class IIActive
Proximal Femoral Locking Plate 020242012
FDA UDI
Class IIActive
7.3mm Cannulated Screw, Long Threaded 060070100
FDA UDI
Class IIActive
Aiming Arm 111223400
FDA UDI
Class IIActive
Proximal Femoral Locking Plate, Combi-holes 020422007
FDA UDI
Class IIActive

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