J & D TECH INC
United States US-MF-000044631 Last updated 23 Oct 2026
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- Devices
- 12
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
Back Brace Ref BB00000001
Walking Cane Ref WC00000001
Shoulder Brace Ref SB00000001
Bathroom Grab Bar Ref BGB0000001
Elbow Brace Ref EB00000001
Knee Brace Ref KB00000001
Arm Sling Ref AS00000001
Arm Brace Ref AB00000001
Wrist Brace Ref WB00000001
Foot Brace Ref FB00000001
Finger Brace Ref FSB0000001
Leg Brace Ref LB00000001
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Authorised representatives
What J & D TECH INC makes
J & D Tech Inc manufactures orthopedic support devices, including braces for the back, shoulders, elbows, knees, arms, wrists, fingers, legs, and feet, as well as assistive mobility aids like walking canes. The company also produces grab bars for bathroom safety and hydrotherapy bath tanks.
These devices are classified as Class I under regulatory frameworks, and the manufacturer lists them in the EU’s eudamed registry. The company is based in the United States.
Frequently asked questions
What types of medical devices does J & D Tech Inc manufacture?
J & D Tech Inc specializes in orthopedic support devices and mobility aids. Their most common products include braces for various body parts—such as back, shoulder, elbow, knee, arm, wrist, finger, leg, and foot—as well as assistive mobility tools like walking canes. They also produce hydrotherapy bath tanks and bathroom grab bars designed to enhance safety and support.
Where is J & D Tech Inc based?
J & D Tech Inc is headquartered in the United States. Their location is relevant for understanding regulatory compliance, manufacturing standards, and potential distribution networks within North America and beyond.
Which regulatory registries list J & D Tech Inc’s devices?
J & D Tech Inc’s devices are listed in the eudamed registry, which is the official EU database for medical devices. Listing in eudamed is required for manufacturers whose products are placed on the European market, ensuring traceability and compliance with EU Medical Device Regulations.
How are J & D Tech Inc’s devices classified under regulatory frameworks?
J & D Tech Inc’s devices are classified as Class I under regulatory schemes like the EU MDR (Medical Device Regulation). Class I devices are generally considered low-risk, often involving items like braces, canes, and grab bars, which typically do not require invasive procedures or sustained implantation.
Information
- Country
- United States
- Address
- 120 LAKE AVE S STE 22,NESCONSET,, NY, United States
- [email protected]
- PRRC contact
- Rong Dang
- EUDAMED SRN
- US-MF-000044631
- FDA FEI number
- 3016579495