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Intai Technology Corporation

US

Last updated May 23, 2026

What Intai Technology Corporation makes

Intai Technology Corporation manufactures reusable surgical instruments for orthopaedic and neurological stereotactic procedures, including bone taps, torque wrenches, drill bits, implant inserters/extractors, mallets, and screwdrivers. Their product line also includes stereotactic surgery systems designed for precision-guided interventions in spinal and cranial surgeries.

The company’s devices are regulated under FDA classifications, with most falling into Class I and Class II categories. Products are listed in the FDA’s 510(k) and UDI registries, reflecting their authorised status for commercial distribution in the US.

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 Intai Technology Corporation manufacture?

Intai Technology Corporation specialises in reusable surgical instruments for orthopaedic and neurological stereotactic procedures. Their product line includes bone taps, torque wrenches, fluted surgical drill bits, implant inserters/extractors, mallets, screwdrivers, and stereotactic surgery systems. These systems are designed for precision-guided interventions in spinal and cranial surgeries, ensuring accuracy during complex procedures.

Where is Intai Technology Corporation based?

Intai Technology Corporation is headquartered in the United States. While the exact location isn’t specified, the company’s regulatory filings and device classifications are aligned with US standards, including FDA requirements.

Which regulatory registries list Intai Technology Corporation’s devices?

Intai Technology Corporation’s devices are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries. These registries track authorised medical devices for commercial distribution in the US, ensuring transparency and compliance with regulatory standards.

How are Intai Technology Corporation’s devices classified under FDA regulations?

Intai Technology Corporation’s devices are primarily classified as Class I or Class II under FDA regulations. Class I devices generally pose minimal risk and may require less stringent controls, while Class II devices involve moderate risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s purpose, intended use, and potential risks.

What distinguishes Intai Technology Corporation’s stereotactic surgery systems from other devices they produce?

Intai Technology Corporation’s stereotactic surgery systems are designed specifically for precision-guided interventions in orthopaedic and neurological surgeries, such as spinal and cranial procedures. Unlike general-purpose reusable instruments like taps, wrenches, or screwdrivers, these systems integrate advanced targeting technology to improve accuracy during complex surgeries, reducing potential errors and enhancing procedural outcomes.

AI-generated from registry data and not verified by a human reviewer.

Information

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US
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Catalogue (55)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
WatchTower INS-GP540L
FDA UDI
Class IActive
WatchTower INS-DRIBIT
FDA UDI
Class IActive
WatchTower INS-NAVSDR
FDA UDI
Class IIActive
WatchTower INS-NAVTAP-001
FDA UDI
Class IActive
WatchTower INS-GUAPIN
FDA UDI
Class IActive
WatchTower INS-HEXWR2
FDA UDI
Class IActive
WatchTower INS-VBLOCK
FDA UDI
Class IIActive
WatchTower INS-NAVAWL
FDA UDI
Class IIActive
WatchTower ROAM SYS-CALI12
FDA UDI
Class IIActive
WatchTower INS-SLDHMR
FDA UDI
Class IActive
WatchTower INS-INSTRA
FDA UDI
Class IActive
WatchTower INS-NAVHDL-A
FDA UDI
Class IIActive
WatchTower ROAM SYS-NAVI02
FDA UDI
Class IIActive
WatchTower INS-NAVTAP-055
FDA UDI
Class IIActive
WatchTower INS-PAMAWL
FDA UDI
Class IIActive
WatchTower INS-TAPC60
FDA UDI
Class IIActive
WatchTower INS-NAVTAP-050
FDA UDI
Class IIActive
WatchTower INS-NAVTAP-065
FDA UDI
Class IIActive
WatchTower NAVTL0004
FDA UDI
Class IIActive
WatchTower INS-POSTWR
FDA UDI
Class IActive
WatchTower INS-REFPIN
FDA UDI
Class IIActive
WatchTower INS-NAVTAP-075
FDA UDI
Class IIActive
WatchTower NAVTL0001
FDA UDI
Class IIActive
WatchTower INS-HEXWR3
FDA UDI
Class IActive
Anatase Spine Surgery Navigation System INS-TAP55D
FDA UDI
Class IIActive
WatchTower INS-BONPIN
FDA UDI
Class IActive
WatchTower INS-NAVTAP-070
FDA UDI
Class IIActive
WatchTower Navi Disposable Instrument SUR-AWL-01
FDA UDI
Class IIActive
WatchTower INS-FIXPIN-001
FDA UDI
Class IActive
WatchTower INS-DRIVER-A
FDA UDI
Class IActive
WatchTower INS-NAVHDL-B
FDA UDI
Class IIActive
WatchTower INS-FIXPIN-002
FDA UDI
Class IActive
WatchTower Navi Disposable Instrument SUR-REF-01
FDA UDI
Class IIActive
WatchTower INS-RATHDL
FDA UDI
Class IIActive
WatchTower INS-GUIAWL
FDA UDI
Class IIActive
WatchTower INS-TAPC50
FDA UDI
Class IIActive
WatchTower INS-RELESR
FDA UDI
Class IActive
WatchTower Navi Disposable Instrument SUR-REF-01-A
FDA UDI
Class IIActive
WatchTower INS-TAPC70
FDA UDI
Class IIActive
WatchTower INS-NAVHDL-C
FDA UDI
Class IIActive
WatchTower INS-NAVTAP-060
FDA UDI
Class IIActive
WatchTower NAVTL0002
FDA UDI
Class IIActive
WatchTower INS-UNIHDL
FDA UDI
Class IIActive
WatchTower SNS-Spine
FDA UDI
Class IIActive
WatchTower INS-DRIB02
FDA UDI
Class IActive
WatchTower INS-NADRGU
FDA UDI
Class IIActive
WatchTower INS-DRIGUI
FDA UDI
Class IIActive
WatchTower INS-DRIVER-B
FDA UDI
Class IActive
WatchTower INS-SDR081
FDA UDI
Class IIActive
WatchTower INS-FIXPIN-003
FDA UDI
Class IActive

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