KEVINROOT MEDICAL

FDA Device Registration & Listing · Riverside, CA, US · Registration 3021443431

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3021443431
FEI Number
3021443431
Entity Name
KEVINROOT MEDICAL
City/State/Country
Riverside, CA, US
Establishment Address
2239 Business Way, Riverside, CA 92501, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
KevinRoot Medical (Owner Number: 10091892)
Owner / Operator Contact Address
2239 Business Way, Riverside, CA 92501, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

CT - Control TL Carbon, CX - Control ,XT Carbon, DP - Dress Polypro, DT - Dress TL Carbon, DX - Dress XT Carbon A9 - Coleman, Carbon Footplate Rigid, Carbon Footplate Semi-Rigid, CE - Control EVA, CP - Control Polypro S16 - Road Cycling, S17 - Mountain Biking, S18 Trail Running, S19 - Figure Skating, S2 Ski Pro L6 - Perseus, L7 - Cobra, L8 - DAS, LP L9 - Coleman, LP M1 - Field, M2 - Garrison, M3 - Leisure S4.5 - Basketball Equipe, S5 - Football, S5.5 Lineman, S6 - Baseball, S7 - Soccer, S8 - Jogging, S9 - Marathon S1 - Ski, S10 - Volleyball, S11 - Tennis, S12 - Water, S13 - Skateboard, S14 - Track & Field, S15 - Golf PP - Performance Polypro, PT - Performance TL Carbon, PX - Performance XT Carbon, Root Acrylic, Root Blake, Root Cobra 3D Design Only, A1 - Pro Sport ,A10 - Easy Flex, A100 - Solid Ankle ,A11 - Cushion Plus T7-A5514 Therapeutic Shoe UCB Type Orthosis A12 - Unit A2 - Carbon Sport, A3 - Classic Sport ,A4 - Subo-Flex, A5 - Supporter ,A6 - Cork & Leather, A7 - Pro EVA A8 P1 - Achilles Tendinopathy, P10 - Pediatric Flatfoot, P11 - Pes Cavus, P12 - Pes Planus, P13 - Plantar Fasciitis P14 - Sesamoiditis, P2 - Adult Acquired Flatfoo,t P3 - Lateral Ankle Instability, P4 - Hallux Limitus, P5 - Hallux Rigid 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 T9 - EVA UCBL, UE- UCBL fit EVA, UP- UCBL fit Polypro, UT- UCBL fit TL Carbon, UX- UCBL fit XT Carbon, Clips and Zip Root Fiberglass, Root Graphite, Root Hole-Heel, Root Men's Dress, Root Modified UCBL, Root Multi-Sport Root SSC, Root Women's Casual, Root Women's High-Heel L1 - Fashion, L10 - High Heels, L2 - Princess, L3 - Ultra Slim, L4 - SuboFlex LP, L5 - Supporter LP T1 - Care Soft, T2 - Care Firm, T3 - Premium Diabetic, T4 - UCBL, T5 - Modified UCBL, T6 - Pediatric UCBL P6 - Heel Spurs, P7 - Intoeing Gait , P8 - Metatarsalgia, P9 - Neuroma, PE - Performance EVA S20 - Ice/Roller Hockey S21 - Hunting & Fishing, S22 - Hiker, S23 - Ultralite Runner, S3 - Snowboard, S4 - Basketball Root Cushion-Flex, Root Cushion-Flex-Control, Root Diaba-Flex, Root Diaba-Flex-Control, Root Dwyer

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2024-11-13

Official Correspondent

Kevin Rosenbloom

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

KevinRoot Medical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3021443431. Last updated year: 2026. Please use registration number 3021443431 when referencing this establishment in official correspondence.
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