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Extreme Liner

FDA UDI

Class I (US FDA UDI)

by Alps South, LLC

Identity

Trade Name
EXTREME LINER FDA UDI
Generic Name
External limb prosthesis socket liner FDA UDI
Device Name
Extreme Liner w/Expulsion Port FDA UDI
Model / Reference
VKDT26-3 FDA UDI
Description
Extreme Liner w/Expulsion Port FDA UDI

Identifiers

Primary DI / UDI-DI
00713980005834 FDA UDI
FDA Product Code
ISS FDA UDI
GMDN Term
External limb prosthesis socket liner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3420 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

No

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: External limb prosthesis socket liner

Extreme Liner by Alps South, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External limb prosthesis socket liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Alps South, LLC

Sources (1)

  • FDA UDI aef4161b-1acf-4456-8072-2cdc260db16c 33 fields · synced May 30, 2026