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FAQ 202 Plus

FDA UDI

Class II (US FDA UDI)

by Foreo Inc

Identity

Trade Name
FAQ 202 Plus FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Device Name
FAQ™ 200 Plus is intended to use LED light for the treatment of wrinkles and mild to moderate acne. FDA UDI
Model / Reference
Black FDA UDI
Description
FAQ™ 200 Plus is intended to use LED light for the treatment of wrinkles and mild to moderate acne. FDA UDI

Identifiers

Primary DI / UDI-DI
07640260120662 FDA UDI
510(k) Number
K240378 FDA UDI
FDA Product Code
OHS FDA UDI
OLP FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blue/red/infrared phototherapy lamp

FAQ 202 Plus by Foreo Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blue/red/infrared phototherapy lamp.

Cleared under the same submission

K240378 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Foreo Inc

Sources (1)

  • FDA UDI 91bcd64f-16f8-4c2e-beee-f414764cb46c 34 fields · synced May 30, 2026