Footmaxx of Virginia

FDA Device Registration & Listing · Roanoke, VA, US · Registration 3009285151

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
3009285151
FEI Number
3009285151
Entity Name
Footmaxx of Virginia
City/State/Country
Roanoke, VA, US
Establishment Address
518 Pocahontas Ave Ne, Roanoke, VA 24012, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Footmaxx of Virginia (Owner Number: 10031149)
Owner / Operator Contact Address
518 Pocahontas Avenue, Roanoke, VA 24012, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Custom Orthopedic Braces Metascan Pressure Mat 3DMaxx Scanner GEN3 3DMaxx Scanner Footmaxx orthotics

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
IPM Cover, Limb Physical Medicine Class 1 890.3025 2013-11-19
KNP Orthosis, Corrective Shoe Physical Medicine Class 1 890.3475 2009-12-24

Official Correspondent

Scott Roupe

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Footmaxx of Virginia
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 3009285151. Last updated year: 2026. Please use registration number 3009285151 when referencing this establishment in official correspondence.
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