← Back to catalogue

Legacy IPC

FDA UDI

Class II (US FDA UDI)

by Ig Technology, Ltd.

Identity

Trade Name
Legacy IPC FDA UDI
Generic Name
Intermittent venous compression system FDA UDI
Device Name
The Legacy® IPC is a prescription device intended for the prophylaxis of Deep Vein Thrombosis (DVT), stimulating venous and arterial circulation, aiding in the prevention of venous stasis ulcers, aiding in the healing of cutaneous ulcers, reducing acute/chronic edema and compartmental pressures. For use in home or hospital settings. FDA UDI
Model / Reference
v1 FDA UDI
Description
The Legacy® IPC is a prescription device intended for the prophylaxis of Deep Vein Thrombosis (DVT), stimulating venous and arterial circulation, aiding in the prevention of venous stasis ulcers, aiding in the healing of cutaneous ulcers, reducing acute/chronic edema and compartmental pressures. For use in home or hospital settings. FDA UDI

Identifiers

Catalog Number
001-000 FDA UDI
Primary DI / UDI-DI
05065012360097 FDA UDI
510(k) Number
K232006 FDA UDI
FDA Product Code
JOW FDA UDI
GMDN Term
Intermittent venous compression system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5800 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

Yes

FDA UDI

Over-the-Counter

No

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
MRI Safety
MR Unsafe FDA UDI

Category: Intermittent venous compression system

Legacy IPC by Ig Technology, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intermittent venous compression system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Ig Technology, Ltd.

Sources (1)

  • FDA UDI c4f45d7c-9eab-4085-9eb0-3f83fd3e941b 36 fields · synced Jun 8, 2026