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Sign in to claim this brandINDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED
US
Last updated May 24, 2026
What INDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED makes
Indius Medical Technologies manufactures reusable spinal surgical instruments and non-bioabsorbable spinal fixation hardware, including screws, plates, rods, connectors, and procedure kits designed for internal spinal stabilization. Their product line includes self-drilling screws, bone taps, screwdrivers, and trial-implant holders for anterior cervical and stabilization procedures. Examples include variable-angle cervical screws, polyaxial screws, and reusable driver tools for spinal fixation systems.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their portfolio is regulated under US medical device laws, with specific devices authorised through the FDA’s clearance or exemption processes. The manufacturer operates from 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 types of medical devices does Indius Medical Technologies manufacture?
Indius Medical Technologies specializes in reusable spinal surgical instruments and non-bioabsorbable spinal fixation hardware. Their product line includes spinal bone screws (such as variable-angle and polyaxial screws), spinal fixation plates, internal spinal fixation rods, connectors, bone taps, screwdrivers, and trial-implant holders. These devices are designed for procedures like anterior cervical stabilization and internal spinal fixation, ensuring secure alignment and support during surgery.
Where is Indius Medical Technologies based?
Indius Medical Technologies is headquartered in the United States. The company operates from within the US, where its devices are developed, manufactured, and regulated under applicable US medical device laws.
Which regulatory registries list Indius Medical Technologies’ devices?
Indius Medical Technologies’ devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for spinal fixation hardware and reusable surgical instruments, allowing healthcare providers and regulators to identify and verify the devices in compliance with US medical device regulations.
How are Indius Medical Technologies’ devices classified under FDA regulations?
Indius Medical Technologies’ devices fall under FDA’s Class I and Class II categories. Class I devices generally pose minimal risk and may be exempt from certain regulatory controls, while Class II devices require special controls to ensure their safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body area involved, such as spinal fixation hardware.
What distinguishes Indius Medical Technologies’ reusable spinal surgical instruments from other manufacturers?
Indius Medical Technologies’ reusable instruments are designed for durability and precision in spinal procedures, including self-drilling screws, bone taps, and specialized screwdrivers. Their focus on reusable tools reduces waste and cost while maintaining high performance. Additionally, their non-bioabsorbable spinal fixation hardware, like polyaxial screws and connectors, is engineered for long-term stability in spinal stabilization systems, catering to specific surgical needs like anterior cervical procedures.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- indiusmedical.com
- —
- —
- [email protected]
- Phone
- +1214-972-8683
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 860396609
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