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Knee Support Orthopedic Knee Brace

FDA UDI

Class I (US FDA UDI)

by Home Aide Diagnostics, Inc.

Identity

Trade Name
Knee Support Orthopedic Knee Brace FDA UDI
Generic Name
Tubular support bandage, non-latex, reusable FDA UDI
Device Name
• Thermal neoprene sleeves • Adjustable VELCRO straps • Fits right or left knee • Rigid uprights for support • Stabilize collateral ligaments • Decreases pain symptoms • Improves joint function • Stabilizes knee joint • Help with Arthritic knee pain FDA UDI
Model / Reference
83101-83106 FDA UDI
Description
• Thermal neoprene sleeves • Adjustable VELCRO straps • Fits right or left knee • Rigid uprights for support • Stabilize collateral ligaments • Decreases pain symptoms • Improves joint function • Stabilizes knee joint • Help with Arthritic knee pain FDA UDI

Identifiers

Catalog Number
1614 FDA UDI
Primary DI / UDI-DI
00891237001614 FDA UDI
FDA Product Code
IQI FDA UDI
GMDN Term
Tubular support bandage, non-latex, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3475 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Tubular support bandage, non-latex, reusable

Knee Support Orthopedic Knee Brace by Home Aide Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tubular support bandage, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f5298ff0-88e9-454c-9522-cd961a3b7f92 35 fields · synced Jun 1, 2026