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Pro Lh80

FDA UDI

Class II (US FDA UDI)

by Theradome, Inc.

Identity

Trade Name
PRO LH80 FDA UDI
Generic Name
Hair growth laser device FDA UDI
Device Name
Theradome PRO LH80 laser helmet is a low level laser therapy (LLT) device containing red, visible light diode lasers operating at 678 nanometers, designed to deliver non-thermal energy to the hair follicles used to promote hair growth via photobiostimultion of the scalp. FDA UDI
Model / Reference
PRO LH80 FDA UDI
Description
Theradome PRO LH80 laser helmet is a low level laser therapy (LLT) device containing red, visible light diode lasers operating at 678 nanometers, designed to deliver non-thermal energy to the hair follicles used to promote hair growth via photobiostimultion of the scalp. FDA UDI

Identifiers

Catalog Number
PRO LH80 FDA UDI
Primary DI / UDI-DI
B399PRO0800 FDA UDI
510(k) Number
K122950 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

Pro Lh80 by Theradome, 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
Theradome, Inc.

Sources (1)

  • FDA UDI 5c890697-9cb2-4f07-9356-b3b218fd9fd2 37 fields · synced May 30, 2026