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Sign in to claim this brandLaserCap Company
US
Last updated May 24, 2026
What LaserCap Company makes
LaserCap Company manufactures non-invasive laser devices designed to stimulate hair growth, including handheld and cap-based systems for targeted or full-scalp treatment. Products vary in laser intensity, coverage area, and design, such as single-device units, multi-device arrays, and wearable caps with adjustable settings. Examples include handheld units like the Turbo LaserCap and cap-based systems like the LaserCap HD+ and Medi Tresse variants, as well as specialized models like the Foundation Light Therapy LaserCap and the ZCap.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the United States, adhering to applicable medical device standards and reporting requirements. No other regulatory registries or jurisdictions are referenced in the product portfolio.
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 LaserCap Company manufacture?
LaserCap Company specializes in non-invasive laser devices designed to promote hair growth. Their portfolio includes handheld laser units like the Turbo LaserCap and cap-based systems such as the LaserCap HD+ and Medi Tresse LaserCap HD, which deliver targeted or full-scalp laser therapy. These devices vary in design, coverage area, and laser intensity to cater to different treatment preferences.
Where is LaserCap Company based, and where are their devices primarily intended for use?
LaserCap Company is based in the United States. Their devices are specifically intended for use in the U.S., where they must comply with applicable medical device regulations, including classification and reporting requirements.
Which regulatory registries list LaserCap Company’s devices?
LaserCap Company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is used to track and identify medical devices authorized for use in the United States. No other regulatory registries or jurisdictions are referenced for their product portfolio.
How are LaserCap Company’s devices classified under FDA regulations?
LaserCap Company’s devices fall under Class II classification according to FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls to ensure their safety and effectiveness, such as laser hair growth devices that require validation of performance and labeling requirements.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- lasercap.com
- —
- —
- [email protected]
- Phone
- 855-424-7774
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 056706029
Catalogue (15)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| LaserCap HD+ | 00850056575003 | FDA UDI | Class II | Active |
| Turbo LaserCap | 00850056575058 | FDA UDI | Class II | Active |
| Medi Tresse LaserCap HD | 00850056575072 | FDA UDI | Class II | Active |
| Medi Tresse LaserCap HD+ | 00850056575065 | FDA UDI | Class II | Active |
| LaserCap SD | 00850056575027 | FDA UDI | Class II | Active |
| Foundation Light Therapy LaserCap | 00850056575119 | FDA UDI | Class II | Active |
| LaserCap HD | 00850056575010 | FDA UDI | Class II | Active |
| LaserCap HD XL | 00850056575034 | FDA UDI | Class II | Active |
| LaserCap MC2 | 00850056575041 | FDA UDI | Class II | Active |
| V8 LaserCap | 00850056575089 | FDA UDI | Class II | Active |
| Get Hair MD LaserCap | 00850056575133 | FDA UDI | Class II | Active |
| ZCap | 00850056575096 | FDA UDI | Class II | Active |
| Foundation Light Therapy Optima LaserCap | 00850056575126 | FDA UDI | Class II | Active |
| CURE LaserCap | 00850056575140 | FDA UDI | Class II | Active |
| Maxim LaserCap | 00850056575102 | FDA UDI | Class II | Active |
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