Stockinet

FDA UDI

Class II (US FDA UDI)

by Normatec Industries, Lp

Identity

Trade Name: Stockinet FDA UDI
Generic Name: Sequential venous compression system FDA UDI
Device Name: Stockinet - 8" FDA UDI
Model / Reference: Stockinet - 8" FDA UDI
Description: Stockinet - 8" FDA UDI

Identifiers

Catalog Number: 30402 FDA UDI
Primary DI / UDI-DI: 00817369020712 FDA UDI
510(k) Number: K013436 FDA UDI
K112890 FDA UDI
FDA Product Code: JOW FDA UDI
IRP FDA UDI
GMDN Term: Sequential venous compression system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5800 FDA UDI
890.5650 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Intermittent venous compression system Sequential venous compression system

Stockinet by Normatec Industries, Lp — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sequential venous compression system.

Mueller Sports Medicine — Mueller Sports Medicine, Inc. · Class II
HYDROVEN — Huntleigh Healthcare , Ltd. · Class II
AeroWrap™ Flex Large — SUN-SCIENTIFIC INC. · Class I
Rapid Reboot Recovery Products — RAPID REBOOT RECOVERY PRODUCTS · Class II
CoreTech — VIVE HEALTH LLC · Class II
AeroWrap™ — SUN-SCIENTIFIC INC. · Class I
Compression Therapy Device — Guangzhou Longest Medical Technology Co., Ltd. · Class II
Aero-Wrap™ Bilateral Kit, Medium — SUN-SCIENTIFIC INC. · 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Normatec Industries, Lp

Sources (1)

FDA UDI 79b45c2f-9f43-4aa6-845a-85d9e784472a 35 fields · synced Jun 1, 2026