What is FDA product code OIZ?

Assist a patient to visualize the image and condition of the soles of their feet in connection with a daily self-examination for signs of inflammation on the sole of the foot. The device will assist the patient in determining when they should contact their healthcare provider for further diagnosis and treatment regarding any skin changes seen by a mirror and/or highlighted by the liquid crystal foot pads. Intended to be used as an adjunct to, and not in replacement of, periodic foot care and examinations conducted by a health care professional and used under the direction of a health care professional and does not diagnose any specific disease state.

Physical Medicine › TherapeuticFoot Examination Tool For Inflammatory Changes

Empo Footprint

Name: Empo Footprint
Brand: Empo Footprint

Catalogue number EM0001, listed by Empo Health, Inc., United States, under Foot Examination Tool For Inflammatory Changes. 1 manufacturer in China is registered for this product code.

Registry build 21.09.26

1manufacturer

1catalogue number

Who Else Makes It

Registered in Zhejiang.

Chinese manufacturers registered for FDA product code OIZ
Manufacturer	City	Province	Registered as	Device types
Ningbo Weifeng Houseware Co., Ltd.	Ningbo	Zhejiang	Manufacturer	5

Record

Regulatory record for Empo Footprint
Listed by	Empo Health, Inc., United States
FDA product code	OIZ
Device type	Foot Examination Tool For Inflammatory Changes
Device class	Class 1
Regulation	21 CFR 890.5050
Establishment	Specification developer, Manufacturer
Premarket notification	Exempt
Record published	2025-07-31
Record revised	2026-03-25 (version 2)

Specifications

Specifications
MRI safety	Labeling does not contain MRI Safety Information
Label carries	serial number

Catalogue Numbers

Catalogue numbers for Empo Footprint
Catalogue number	Size	Status
EM0001		In distribution

Same Product Code

Other products under the same FDA product code
Product	Sold by	Catalogue numbers
Podimetrics SmartMat+	Podimetrics, Inc.	2
Podimetrics Remanufactured SmartMat	Podimetrics, Inc.	1
Bluedrop Medical	Bluedrop Medical Ltd	1
Podimetrics Wi-Fi SmartMat	Podimetrics, Inc.	1
Orpyx Sensory Insoles	Orpyx Medical Technologies Inc.	1

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.