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Sign in to claim this brandDREAM FACTORY INC.
US
Last updated May 25, 2026
What DREAM FACTORY INC. makes
Dream Factory Inc. manufactures hand-held electric massagers designed for muscle relaxation and pliability training. Their products include vibrating spheres, rollers, and mini spheres intended for targeted tissue stimulation and mobility support.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 types of medical devices does Dream Factory Inc. manufacture?
Dream Factory Inc. specializes in hand-held electric massagers. These devices are designed for muscle relaxation and pliability training, with examples including vibrating spheres, rollers, and mini spheres. The products focus on targeted tissue stimulation and mobility support.
Where is Dream Factory Inc. based?
Dream Factory Inc. is headquartered in the United States. The company’s location is relevant for regulatory compliance and customer inquiries, as it operates within the U.S. medical device landscape.
How are Dream Factory Inc.’s devices classified under FDA regulations?
Dream Factory Inc.’s hand-held electric massagers fall under Class I classification by the FDA. This classification is typically assigned to low-risk devices that pose minimal potential harm to users, requiring fewer regulatory controls compared to higher-risk categories.
Are Dream Factory Inc.’s devices listed in any regulatory registries?
Yes, Dream Factory Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. Listing in the UDI system ensures traceability and transparency for regulatory tracking, helping healthcare providers and authorities verify device details like manufacturer information and compliance status.
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
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- DUNS Number
- 698505802
Catalogue (3)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Tb12 Vibrating Pliability Mini Sphere | VMINI-BLK-01A | FDA UDI | Class I | Active |
| Tb12 Vibrating Pliability Roller | VPLI-RED-02A | FDA UDI | Class I | Active |
| Tb12 Vibrating Pliability Sphere | VBALL-BLK-02A | FDA UDI | Class I | Active |
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