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Faq 302

FDA UDI

Class II (US FDA UDI)

by Foreo Inc

Identity

Trade Name
FAQ 302 FDA UDI
Generic Name
Hair growth laser device FDA UDI
Device Name
FAQ 302 is indicated to promote hair growth in males with androgenetic alopecia who have Hamilton-Norwood Classifications of Ila-V and females with androgenetic alopecia who have Ludwig-Savin Classifications of l-II and Fitzpatrick Classification of Skin Phototypes I to IV. FDA UDI
Model / Reference
Black Diamond FDA UDI
Description
FAQ 302 is indicated to promote hair growth in males with androgenetic alopecia who have Hamilton-Norwood Classifications of Ila-V and females with androgenetic alopecia who have Ludwig-Savin Classifications of l-II and Fitzpatrick Classification of Skin Phototypes I to IV. FDA UDI

Identifiers

Primary DI / UDI-DI
07640260120297 FDA UDI
510(k) Number
K242747 FDA UDI
FDA Product Code
OAP FDA UDI
GMDN Term
Hair growth laser device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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: Hair growth laser device

Faq 302 by Foreo Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hair growth laser device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Foreo Inc

Sources (1)

  • FDA UDI 6d5d0404-a8f9-4bc2-9b2d-5aba8d921934 34 fields · synced Jun 8, 2026