KIWI Derma

FDA UDI

Class I (US FDA UDI)

by Foreo Inc

Identity

Trade Name: KIWI Derma FDA UDI
Generic Name: Dermabrasion brush, rotary FDA UDI
Device Name: KIWI Derma is blackhead suction device with microdermabrasion nozzle to remove dead skin and with T-sonic pulsation to suck out blackhead more easily. FDA UDI
Model / Reference: Lavender FDA UDI
Description: KIWI Derma is blackhead suction device with microdermabrasion nozzle to remove dead skin and with T-sonic pulsation to suck out blackhead more easily. FDA UDI

Identifiers

Primary DI / UDI-DI: 07350120791955 FDA UDI
FDA Product Code: KNM FDA UDI
GMDN Term: Dermabrasion brush, rotary FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5765 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

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dermabrasion brush, rotary

KIWI Derma by Foreo 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: Foreo Inc

Sources (1)

FDA UDI f9d3fd48-43de-4c48-98d0-476b5212bba7 33 fields · synced Jun 8, 2026