POD Active Knee Brace

FDA UDI

Class I (US FDA UDI)

by Pod Active Pty Ltd

Identity

Trade Name: POD Active Knee Brace FDA UDI
Generic Name: Knee support orthosis FDA UDI
Device Name: POD Active Knee Brace; model K8; version 3.0; pairs (LT & RT) FDA UDI
Model / Reference: K8 3.0 (Pairs) FDA UDI
Description: POD Active Knee Brace; model K8; version 3.0; pairs (LT & RT) FDA UDI

Identifiers

Catalog Number: K8300## FDA UDI
Primary DI / UDI-DI: 09344006000840 FDA UDI
FDA Product Code: ITQ FDA UDI
GMDN Term: Knee support orthosis 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Knee support orthosis

POD Active Knee Brace by Pod Active Pty Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Knee support orthosis.

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MEDI — MEDI MANUFACTURING, INC. · Class I
MEDI — MEDI MANUFACTURING, INC. · Class I
NON FRANCHISE — DJO, LLC · Class I
DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
Gripper Hinged Knee — MEDICAL SPECIALTIES INCORPORATED · Class I
DeRoyal — DEROYAL INDUSTRIES, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Pod Active Pty Ltd

Sources (1)

FDA UDI 6f0dd785-5115-4aab-abd7-d36d02914b51 36 fields · synced May 31, 2026