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Core-Spun®

FDA UDI

Class I (US FDA UDI)

by Knit-Rite, Inc

Identity

Trade Name
Core-Spun® FDA UDI
Generic Name
Compression/pressure sock/stocking, single-use FDA UDI
Device Name
15-20 mmHg CORESPUN SOCKS LARGE SHORT KHAKI FDA UDI
Model / Reference
17531 FDA UDI
Description
15-20 mmHg CORESPUN SOCKS LARGE SHORT KHAKI FDA UDI

Identifiers

Primary DI / UDI-DI
00721734175313 FDA UDI
FDA Product Code
FQL FDA UDI
DWL FDA UDI
GMDN Term
Compression/pressure sock/stocking, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5780 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

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: Compression/pressure sock/stocking, single-use

Core-Spun compression socks are designed to provide targeted pressure and support for individuals with circulation-related disorders, such as venous insufficiency or deep vein thrombosis. These single-use compression stockings feature a unique blend of elastic materials and graduated compression technology, making them an effective solution for home or clinical use.

Similar devices

Also classified as Compression/pressure sock/stocking, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Knit-Rite, Inc

Sources (1)

  • FDA UDI 971d7fcf-7265-4f3f-8ed5-e8e0cacd389d 33 fields · synced Jul 25, 2026