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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 Women Firm Support (20-30 mmHg) Knee Length, Closed Toe FDA UDI
Model / Reference
DSL-7110-BGL1 Beige Large FDA UDI
Description
Graduated Compression Support Sock for Women Firm Support (20-30 mmHg) Knee Length, Closed Toe FDA UDI

Identifiers

Primary DI / UDI-DI
00042825534841 FDA UDI
510(k) Number
K123398 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

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

Similar devices

Also classified as Compression/pressure sock/stocking, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Renfro Corporation

Sources (1)

  • FDA UDI e305299d-9ebc-442b-8321-0ad3c61340d8 35 fields · synced May 30, 2026