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Sign in to claim this brandBLISSCO MEDICAL DEVICE LIMITED
US
Last updated May 31, 2026
What BLISSCO MEDICAL DEVICE LIMITED makes
Blissco Medical Device Limited manufactures laser-based devices designed to promote hair growth, including wearable caps that use laser technology for targeted treatment. These products are intended for non-invasive use on the scalp to stimulate hair follicles.
The company’s portfolio is classified under FDA’s Class II regulatory category and is listed in the FDA’s Unique Device Identifier (UDI) database. The devices are intended for commercial distribution within 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 Blissco Medical Device Limited manufacture?
Blissco Medical Device Limited specializes in laser-based devices focused on hair growth. Their primary product category is hair growth laser devices, including wearable caps like the Laser Hair Growth Cap and the GWODE Laser Hair Growth Cap. These devices use laser technology to stimulate hair follicles non-invasively on the scalp.
Where is Blissco Medical Device Limited based, and where are their devices intended for use?
Blissco Medical Device Limited is based in the United States. Their devices are designed for commercial distribution within the US market, adhering to applicable regulatory requirements for that jurisdiction.
Which regulatory registries or databases list Blissco Medical Device Limited’s devices?
Blissco Medical Device Limited’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the United States, ensuring transparency and traceability.
How are Blissco Medical Device Limited’s devices classified under regulatory standards?
Blissco Medical Device Limited’s devices fall under the FDA’s Class II regulatory classification. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as laser-based hair growth devices.
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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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
- —
- DUNS Number
- 989184851
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Laser Hair Growth Cap | 1.0 | FDA UDI | Class II | Active |
| GWODE Laser Hair Growth Cap | 1.0 | FDA UDI | Class II | Active |
| Neocontrol Pelvic Floor Therapy System, Incontinence Treatment Device | LT2061 | FDA UDI | Class II | Unknown |
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