Dr. Scholl's

FDA UDI

Class II (US FDA UDI)

by Renfro Corporation

Identity

Trade Name: Dr. Scholl's FDA UDI
Generic Name: Compression/pressure sock/stocking, reusable FDA UDI
Device Name: Graduated Compression Support Sock for Men Moderate Support (15-20 mmHg) Knee Length, Closed Toe FDA UDI
Model / Reference: DSM-7000-BXL1-SK FDA UDI
Description: Graduated Compression Support Sock for Men Moderate Support (15-20 mmHg) Knee Length, Closed Toe FDA UDI

Identifiers

Primary DI / UDI-DI: 00042825634039 FDA UDI
FDA Product Code: DWL FDA UDI
GMDN Term: Compression/pressure sock/stocking, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5780 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

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: Compression/pressure sock/stocking, reusable

Dr. Scholl's by Renfro Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Renfro Corporation

Sources (1)

FDA UDI 243488de-69fa-4383-bd12-af219cc852e9 34 fields · synced May 30, 2026