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iRestore

FDA UDI

Class II (US FDA UDI)

by Freedom Laser Therapy, Inc.

Identity

Trade Name
iRestore FDA UDI
Generic Name
Hair growth laser device FDA UDI
Device Name
The iRestore Professional 282 is indicated to promote hair growth in males who have Norwood-Hamilton Classifications of IIa-V and in females with androgenetic alopecia who have Ludwig-Savin Classifications I-II, and in both with Fitzpatrick Skin Phototypes I-IV. FDA UDI
Model / Reference
ID-505 FDA UDI
Description
The iRestore Professional 282 is indicated to promote hair growth in males who have Norwood-Hamilton Classifications of IIa-V and in females with androgenetic alopecia who have Ludwig-Savin Classifications I-II, and in both with Fitzpatrick Skin Phototypes I-IV. FDA UDI

Identifiers

Primary DI / UDI-DI
00859690003675 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

Yes

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

iRestore by Freedom Laser Therapy, 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

Sources (1)

  • FDA UDI e9d200bd-840f-4f4f-9c59-19252be9acfa 33 fields · synced May 30, 2026