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Capillus

FDA UDI

Class II (US FDA UDI)

by Capillus, LLC

Identity

Trade Name
Capillus FDA UDI
Generic Name
Hair growth laser device FDA UDI
Device Name
Laser cap for the use of promoting hair growth through photobiomodulation FDA UDI
Model / Reference
Pro S2 FDA UDI
Description
Laser cap for the use of promoting hair growth through photobiomodulation FDA UDI

Identifiers

Primary DI / UDI-DI
00810045461526 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

Capillus by Capillus, LLC — 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
Capillus, LLC

Sources (1)

  • FDA UDI ee20de5e-1638-4c65-8189-fe56b3cf668c 33 fields · synced May 29, 2026