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Tanses Technologies Inc

US

Last updated May 24, 2026

What Tanses Technologies Inc makes

Tanses Technologies Inc manufactures ultraviolet tanning devices and professional red-light phototherapy units. Their product line includes tanning beds and booths, such as the T-32 Series and T-44 Series, as well as red-light phototherapy systems like the T-52 Series and TT-50 Series.

These devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI databases. The company 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 types of medical devices does Tanses Technologies Inc manufacture?

Tanses Technologies Inc specializes in two primary categories of devices: ultraviolet tanning devices and professional red-light phototherapy units. Their ultraviolet tanning devices include tanning beds and booths, such as the T-32 Series and T-44 Series, while their red-light phototherapy units are designed for professional use, including models like the T-52 Series and TT-50 Series. These devices are intended for controlled exposure to specific wavelengths of light for cosmetic or therapeutic purposes.

Where is Tanses Technologies Inc based?

Tanses Technologies Inc is headquartered in the United States. The company’s location is relevant for understanding regulatory frameworks, as its devices are subject to U.S. regulatory requirements, including those set by the FDA.

How are Tanses Technologies Inc’s devices classified under FDA regulations?

Tanses Technologies Inc’s devices are classified as Class II under FDA regulations. This classification typically indicates that the devices pose moderate risk and require special controls in addition to general controls to ensure their safety and effectiveness. Class II devices often require pre-market notification (510(k)) submissions to demonstrate substantial equivalence to a legally marketed predicate device.

Which regulatory registries or databases list Tanses Technologies Inc’s devices?

Tanses Technologies Inc’s devices are listed in the FDA’s 510(k) database and the FDA’s Unique Device Identification (UDI) system. The 510(k) database tracks pre-market submissions for Class II devices, while the UDI system ensures standardized identification of medical devices for tracking, traceability, and regulatory compliance. These listings help healthcare providers, regulators, and other stakeholders verify the authorized status of specific devices.

Why are Tanses Technologies Inc’s devices included in the FDA’s UDI system?

The FDA’s Unique Device Identification (UDI) system assigns a unique identifier to medical devices to improve tracking, reduce medical errors, and enhance transparency in the healthcare system. Since Tanses Technologies Inc’s devices are classified as Class II, they are subject to UDI requirements to ensure accurate labeling, traceability, and compliance with post-market surveillance regulations. This system helps streamline regulatory oversight and supports patient safety initiatives.

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

Information

Country
US
Address
—
Website
tanses.com
LinkedIn
—
Facebook
—
Phone
450-622-4004
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
253238190

Catalogue (41)

DeviceModel / ReferenceRegistriesClassStatus
Tanses T-32 Series T-32-160-F
FDA UDI
Class IIActive
Tanses T-44 Series Tx-44-3F
FDA UDI
Class IIActive
Tanses T-32 Series T-32-3F
FDA UDI
Class IIActive
Tanses T-52 Series T-52-M-3F
FDA UDI
Class IIActive
Tanses T-32 Series Tx-32-160-2F
FDA UDI
Class IIActive
Tanses T-52 Series T-52-M
FDA UDI
Class IIActive
Tanses TT-50 Series TT-50
FDA UDI
Class IIActive
Tanses T-32 Series T-32
FDA UDI
Class IIActive
Tanses T-52 Series T-52-M-F
FDA UDI
Class IIActive
Tanses TT-50 Series TT-50/40
FDA UDI
Class IIActive
Tanses T-32 Series T-32-160-3F
FDA UDI
Class IIActive
Tanses T-32 Series T-32-2F
FDA UDI
Class IIActive
Tanses T-40 Series T-40
FDA UDI
Class IIActive
Tanses T-52 Series T-52
FDA UDI
Class IIActive
Tanses T-32 Series TX-32-3F
FDA UDI
Class IIActive
Tanses T-32 Series TX-32
FDA UDI
Class IIActive
Collagentex Series RX-1-Seat
FDA UDI
Class IIActive
Tanses T-72 Series Vector-3F
FDA UDI
Class IIActive
Tanses T-72 Series T-72
FDA UDI
Class IIActive
Tanses T-32 Series T-32-200-3F
FDA UDI
Class IIActive
Collagentex Series RX-1
FDA UDI
Class IIActive
Collagentex Series Rx-2
FDA UDI
Class IIActive
Tanses T-32 Series TX-32-160
FDA UDI
Class IIActive
Tanses T-32 Series T-32-160-2F
FDA UDI
Class IIActive
Tanses T-40 Series T-40-3F
FDA UDI
Class IIActive
Tanses T-44 Series Tx-44
FDA UDI
Class IIActive
Tanses T-32 Series TX-32-160-F
FDA UDI
Class IIActive
Tanses T-32 Series Tx-32-200
FDA UDI
Class IIActive
Tanses T-32 Series T-32-F
FDA UDI
Class IIActive
Tanses TT-50 Series TT-50/45
FDA UDI
Class IIActive
Tanses T-32 Series TX-32-160-3F
FDA UDI
Class IIActive
Collagentex Series Rx-3
FDA UDI
Class IIActive
Tanses T-32 Series T-32-160
FDA UDI
Class IIActive
Tanses T-32 Series TX-32-2F
FDA UDI
Class IIActive
Tanses T-32 Series Tx-32-200-3F
FDA UDI
Class IIActive
Tanses T-40 Series T-40-F
FDA UDI
Class IIActive
Collagentex Series Rx-6
FDA UDI
Class IIActive
Tanses T-32 Series TX-32-F
FDA UDI
Class IIActive
Tanses T-32 Series T-32-200
FDA UDI
Class IIActive
Collagentex Rx-1 K162022
FDA 510(k)
Class IIActive
Collagentex Rx-6 K180585
FDA 510(k)
Class IIActive

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Tanses Technologies, Inc. FABREVILLE Quebec · CA FEI 3003571423