GOGO by THERAFIRM®

FDA UDI

Class I (US FDA UDI)

by Knit-Rite, Inc

Identity

Trade Name: GOGO by THERAFIRM® FDA UDI
Generic Name: Compression/pressure sock/stocking, single-use FDA UDI
Device Name: GOGO TRAVEL SOCKS 3 pack- Sky Points, Berry Stripes, Black Out 15-20 LG FDA UDI
Model / Reference: 24435 FDA UDI
Description: GOGO TRAVEL SOCKS 3 pack- Sky Points, Berry Stripes, Black Out 15-20 LG FDA UDI

Identifiers

Primary DI / UDI-DI: 00721734244354 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

FDA UDI

Single Use

Yes

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

Yes

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

FDA UDI

Category: Compression/pressure sock/stocking, single-use

GOGO by THERAFIRM® by Knit-Rite, Inc — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Knit-Rite, Inc

Sources (1)

FDA UDI 5539c5a1-2cc0-40a7-9166-10a4e0e4c4d5 33 fields · synced Jun 8, 2026