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Sign in to claim this brandSLO LIVING LLC
US
Last updated September 17, 2026
What SLO LIVING LLC makes
SLO Living LLC manufactures orthotic devices designed to correct and support hallux valgus, commonly known as bunions. Their products include padded booties and orthoses that provide alignment and relief for the metatarsophalangeal joint, aiming to reduce discomfort and improve mobility for affected individuals.
The company’s devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identification (UDI) system. 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 SLO Living LLC manufacture?
SLO Living LLC specializes in orthotic devices focused on addressing hallux valgus, commonly referred to as bunions. Their primary product category is the hallux valgus metatarsophalangeal orthosis, which includes padded booties like the Bunion Bootie and BunionETTE Bootie. These devices are designed to provide alignment support and relief for the affected joint, helping to reduce discomfort and improve mobility.
Where is SLO Living LLC based, and where are their devices intended for use?
SLO Living LLC is based in the United States. Their devices are specifically intended for use within the U.S. market, where they must comply with applicable medical device regulations.
How are SLO Living LLC’s devices classified under FDA regulations?
SLO Living LLC’s devices fall under Class I classification according to FDA regulations. This classification is typically assigned to low-risk devices, such as certain orthotics, where general controls are sufficient to ensure safety and effectiveness. The classification is determined based on the intended use and risk profile of the device.
Are SLO Living LLC’s devices listed in any regulatory registries?
Yes, SLO Living LLC’s devices are included in the FDA’s Unique Device Identification (UDI) system. Listing in the UDI database helps ensure traceability and transparency in the medical device supply chain, allowing for better tracking of devices like their hallux valgus orthoses.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 871 Coronado Center Dr Ste 200, Henderson, NV, 89052
- Website
- bunionbootie.com
- —
- —
- [email protected]
- Phone
- 877-208-4540
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3009560916
- DUNS Number
- 078436895
Catalogue (16)
| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Bunion Bootie | XSmallLeft | FDA UDI | Class I | Active |
| Bunion Bootie | LargeRight | FDA UDI | Class I | Active |
| Bunion Bootie | SmallLeft | FDA UDI | Class I | Active |
| Bunion Bootie | LargeLeft | FDA UDI | Class I | Active |
| BunionETTE Bootie | SmallRight | FDA UDI | Class I | Active |
| Bunion Bootie | XSmallRight | FDA UDI | Class I | Active |
| Bunion Bootie | XLargeRight | FDA UDI | Class I | Active |
| BunionETTE Bootie | MediumRight | FDA UDI | Class I | Active |
| BunionETTE Bootie | SmallLeft | FDA UDI | Class I | Active |
| Bunion Bootie | SmallRight | FDA UDI | Class I | Active |
| Bunion Bootie | MediumRight | FDA UDI | Class I | Active |
| Bunion Bootie | MediumLeft | FDA UDI | Class I | Active |
| BunionETTE Bootie | LargeRight | FDA UDI | Class I | Active |
| BunionETTE Bootie | MediumLeft | FDA UDI | Class I | Active |
| BunionETTE Bootie | LargeLeft | FDA UDI | Class I | Active |
| Bunion Bootie | XLargeLeft | FDA UDI | Class I | Active |
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