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Sign in to claim this brandFacemaster of Beverly Hills, Inc.
US
Last updated May 31, 2026
What Facemaster of Beverly Hills, Inc. makes
Facemaster of Beverly Hills, Inc. manufactures transcutaneous neuromuscular electrical stimulation (TENS) systems designed for physical therapy, specifically targeting facial toning. Their devices are marketed as the FaceMaster and FaceMaster Facial Toning System, which deliver electrical impulses to stimulate muscle contraction in the facial region.
The company’s portfolio is classified under FDA’s Class II regulatory category, with devices listed under the 510(k) and Unique Device Identifier (UDI) programs. These products are authorised for commercial distribution in the United States, where the manufacturer is based.
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 Facemaster of Beverly Hills, Inc. manufacture?
Facemaster of Beverly Hills, Inc. specializes in transcutaneous neuromuscular electrical stimulation (TENS) systems designed for physical therapy. Their primary focus is on devices that deliver electrical impulses to stimulate muscle contraction, specifically for facial toning. The company’s portfolio includes systems like the FaceMaster and FaceMaster Facial Toning System.
Where is Facemaster of Beverly Hills, Inc. based, and where are their devices authorised for use?
Facemaster of Beverly Hills, Inc. is based in the United States. Their devices are authorised for commercial distribution in the US, where they are regulated under FDA programs. The company does not manufacture or distribute devices outside the US based on the provided information.
Which regulatory registries or programs list Facemaster of Beverly Hills, Inc.’s devices?
Facemaster of Beverly Hills, Inc.’s devices are listed under the FDA’s 510(k) premarket notification program and the Unique Device Identifier (UDI) system. These registries ensure traceability and compliance with US regulatory requirements for Class II devices.
How are Facemaster of Beverly Hills, Inc.’s devices classified by regulatory authorities?
Facemaster of Beverly Hills, Inc.’s devices fall under the FDA’s Class II regulatory category. This classification is typically assigned to devices that pose moderate risk and require special controls to ensure safety and effectiveness, such as electrical stimulation systems for physical therapy.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- slccompanies.com
- —
- —
- [email protected]
- Phone
- 8007702571
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 014107160
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| FaceMaster | Platinum | FDA UDI | Class II | Active |
| FaceMaster | Platinum | FDA UDI | Class II | Active |
| Facemaster Facial Toning System | K040871 | FDA 510(k) | Class II | Active |
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