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Core-Spun®

FDA UDI

Class II (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
10-15 mmHg CORESPUN SOCKS SMALL WHITE FDA UDI
Model / Reference
16112 FDA UDI
Description
10-15 mmHg CORESPUN SOCKS SMALL WHITE FDA UDI

Identifiers

Primary DI / UDI-DI
00721734161125 FDA UDI
FDA Product Code
DWL FDA UDI
FQL FDA UDI
GMDN Term
Compression/pressure sock/stocking, single-use 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

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 socks are a type of compression or pressure garment used to treat or prevent conditions such as venous insufficiency, deep vein thrombosis (DVT), and swelling in the legs.

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 43e9903d-ca24-48b4-a4a1-ee12248f867d 33 fields · synced Jul 21, 2026