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
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Also classified as Compression/pressure sock/stocking, reusable.
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- Female compression bodystocking — Eto Garments ApS · Class I
Cleared under the same submission
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 e305299d-9ebc-442b-8321-0ad3c61340d8 35 fields · synced May 30, 2026