FDA Device Establishments · JSON-LD · Markdown
FEI 3021443431 · Manufacture Medical Device · Status: Active
| FEI Number | 3021443431 |
|---|---|
| Owner / Operator | KevinRoot Medical (#10091892) |
| Address | 2239 Business Way, Riverside, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KNP |
| Regulation § (21 CFR) | 890.3475 |
| Proprietary names | Root SSC, Root Women's Casual, Root Women's High-Heel; P6 - Heel Spurs, P7 - Intoeing Gait , P8 - Metatarsalgia, P9 - Neuroma, PE - Performance EVA; S16 - Road Cycling, S17 - Mountain Biking, S18 Trail Running, S19 - Figure Skating, S2 Ski Pro; A9 - Coleman, Carbon Footplate Rigid, Carbon Footplate Semi-Rigid, CE - Control EVA, CP - Control Polypro; T7.1 -Diabetic Inserts 1 Pr, 2, 3 prs, T7.1- Diabetic Inserts w/ Bilateral Filler T7.1- Diabetic Inserts w/ Unilateral; Root Multi-Sport-Plus, Root PolyMax, Root Polypropylene, Root Polypropylene, Root Soft-Sport, Root Soft-Sport-Flex; Root Cushion-Flex, Root Cushion-Flex-Control, Root Diaba-Flex, Root Diaba-Flex-Control, Root Dwyer; PP - Performance Polypro, PT - Performance TL Carbon, PX - Performance XT Carbon, Root Acrylic, Root Blake, Root Cobra; A12 - Unit A2 - Carbon Sport, A3 - Classic Sport ,A4 - Subo-Flex, A5 - Supporter ,A6 - Cork & Leather, A7 - Pro EVA A8; CT - Control TL Carbon, CX - Control ,XT Carbon, DP - Dress Polypro, DT - Dress T |
Source: openFDA. Public-domain (CC0).