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US
Last updated May 30, 2026
What SPECTRUM BRANDS, INC. makes
Spectrum Brands, Inc. manufactures intense pulsed light (IPL) systems designed for skin surface treatments, including devices like the Luma Rx and Remington-branded products. These systems are primarily used for cosmetic procedures such as hair removal, skin rejuvenation, and vascular lesion treatment.
The company’s IPL devices fall under FDA Class II regulation 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 compliance standards.
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 Spectrum Brands, Inc. manufacture?
Spectrum Brands, Inc. specializes in intense pulsed light (IPL) skin surface treatment systems. These devices are primarily used for cosmetic applications such as hair removal, skin rejuvenation, and treatment of vascular lesions. The company’s portfolio includes products like the Luma Rx and Remington-branded IPL systems, which are designed to target specific skin concerns with controlled light energy.
Where is Spectrum Brands, Inc. based, and where are its devices intended for use?
Spectrum Brands, Inc. is based in the United States. Its IPL devices are manufactured and intended for use within the U.S. market, where they must comply with applicable medical device regulations, including those set by the FDA.
Which regulatory registries or databases list Spectrum Brands, Inc.’s devices?
Spectrum Brands, Inc.’s IPL 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 U.S., ensuring transparency and traceability for healthcare providers and regulators.
How are Spectrum Brands, Inc.’s devices classified by regulatory authorities?
The company’s IPL systems fall under FDA Class II classification. This classification indicates that while the devices pose moderate risk, they require special controls beyond general controls to ensure their safety and effectiveness, such as performance standards or post-market surveillance.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- xx.xx
- —
- —
- [email protected]
- Phone
- 800-736-4648
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 001951946
Catalogue (17)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Luma Rx | IPL6800R | FDA UDI | Class II | Active |
| Remington | SP7SB | FDA UDI | Class II | Active |
| Remington Products | IPL6000Q | FDA UDI | Class II | Active |
| Remington Products | IPL6000Q-R | FDA UDI | Class II | Active |
| Remington | IPL7510 | FDA UDI | Class II | Active |
| Luma Rx | SP6800FC | FDA UDI | Class II | Active |
| Remington | IPL7000 | FDA UDI | Class II | Active |
| Luma Rx | IPL6800USA | FDA UDI | Class II | Active |
| Luma Rx | SP6800SB | FDA UDI | Class II | Active |
| Luma Rx | SP6800BC | FDA UDI | Class II | Active |
| Remington Products | SP6000SB | FDA UDI | Class II | Active |
| Remington Products | IPL6000USA | FDA UDI | Class II | Active |
| Remington | IPL2000USA | FDA UDI | Class II | Active |
| Remington | SP2000HR | FDA UDI | Class II | Active |
| Remington | IPL2500USA | FDA UDI | Class II | Active |
| Remington Products | IPL6500QFB | FDA UDI | Class II | Active |
| Remington Products | SP6000Q | FDA UDI | Class II | Active |
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