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Sign in to claim this brandShenzhen Ishine Technology Company Limited
US
Last updated May 23, 2026
What Shenzhen Ishine Technology Company Limited makes
Shenzhen Ishine Technology Company Limited manufactures home-use intense pulsed light hair removal units, including devices such as the IPL Hair Removal Device with model numbers skn001, skn005, skn006, skn002, and RoseSkinCo Lumi.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries; 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 does Shenzhen Ishine Technology Company Limited make?
Shenzhen Ishine Technology Company Limited manufactures home-use intense pulsed light hair removal units, including devices such as the IPL Hair Removal Device with model numbers skn001, skn005, skn006, skn002, and RoseSkinCo Lumi. These are the primary products described in the provided data, and no other devices or product lines are mentioned.
Where is Shenzhen Ishine Technology Company Limited based?
Shenzhen Ishine Technology Company Limited is based in the United States, as explicitly stated in the COUNTRY field of the device data. This indicates the company's location for regulatory and operational purposes, though no specific city or address is provided.
Which regulatory registries list the devices made by Shenzhen Ishine Technology Company Limited?
The devices manufactured by Shenzhen Ishine Technology Company Limited are listed in the FDA 510(k) and FDA UDI registries, as indicated in the LISTED IN field. These registries are used to track medical devices cleared for market in the United States, and the company's devices appear in both.
How are the devices made by Shenzhen Ishine Technology Company Limited classified?
The devices made by Shenzhen Ishine Technology Company Limited are classified as Class II medical devices, as stated in the DEVICE CLASSES field. This classification reflects their risk level and regulatory requirements under FDA rules, meaning they require special controls to ensure safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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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
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Catalogue (5)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ishine | skn005 | FDA UDI | Class II | Active |
| ishine | RoseSkinCo Lumi | FDA UDI | Class II | Active |
| ishine | skn006 | FDA UDI | Class II | Active |
| ishine | skn001 | FDA UDI | Class II | Active |
| IPL Hair Removal Device, Model(s): skn001, skn005, skn006, skn002, RoseSkinCo Lumi | K222537 | FDA 510(k) | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Shenzhen Ishine Technology Company Limited Shenzhen Guangdong · CN FEI 3021338880