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Rhein Laser Technologies Co., Ltd.

US

Last updated May 30, 2026

What Rhein Laser Technologies Co., Ltd. makes

Rhein Laser Technologies Co., Ltd. manufactures dermatological diode laser systems for skin treatments and laser lithotripsy systems for breaking down kidney stones. Their portfolio includes devices like the TitanPico Laser Workstation, designed for precise dermatological procedures, and the Artemis Diode Laser System, used for various skin conditions. They also produce Medical Thulium Fiber Laser Systems, such as the UroFiber 60Q, specifically for lithotripsy applications.

The company’s devices fall under Class II regulatory classification in the US, requiring premarket notification (510(k)) or de novo pathways for authorisation. These products are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries. Rhein Laser Technologies Co., Ltd. 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 Rhein Laser Technologies Co., Ltd. manufacture?

Rhein Laser Technologies Co., Ltd. specializes in the production of dermatological diode laser systems and laser lithotripsy systems. Their product range includes the TitanPico Laser Workstation for skin treatments, the Artemis Diode Laser System for various skin conditions, and Medical Thulium Fiber Laser Systems like the UroFiber 60Q, which are used for breaking down kidney stones.

Where is Rhein Laser Technologies Co., Ltd. based?

Rhein Laser Technologies Co., Ltd. is based in the United States. This location is where the company conducts its manufacturing operations for its range of dermatological and lithotripsy laser systems.

How are the devices from Rhein Laser Technologies Co., Ltd. classified and where are they listed?

The devices manufactured by the company are classified as Class II medical devices in the United States. Because of this classification, these products are subject to regulatory oversight and are listed in the FDA 510(k) and Unique Device Identifier (UDI) registries, which track authorized medical equipment.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
704587822

Catalogue (8)

DeviceModel / ReferenceRegistriesClassStatus
TitanPico Laser Workstation PICO-450
FDA UDI
Class IIActive
Artemis Diode Laser System RL-S20S-TWC
FDA UDI
Class IIActive
Medical Thulium Fiber Laser Systems UroFiber 60Q
FDA UDI
Class IIActive
Artemis Diode Laser System RL-S20S-755
FDA UDI
Class IIActive
Artemis Diode Laser System RL-S20S-810B
FDA UDI
Class IIActive
Artemis Diode Laser System (RL-S20S-TWC, RL-S20S-810B, RL-S20S-755) K233756
FDA 510(k)
Class IIActive
TitanPico Laser Workstation (PICO-450) K233757
FDA 510(k)
Class IIActive
Medical Thulium Fiber Laser Systems (UroFiber 60Q) K242293
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

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Authorities

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FDA Establishments (1)

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

  • Rhein Laser Technologies Co., Ltd. wuhan Hubei · CN FEI 3026038437