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Del Sol Red Light Therapy System

FDA UDI

Class II (US FDA UDI)

by Hydrafacial LLC

Identity

Trade Name
Del Sol Red Light Therapy System FDA UDI
Generic Name
Cosmetic red-light phototherapy system, professional FDA UDI
Device Name
Del Sol Red Cordless LED Light for EU/CE only FDA UDI
Model / Reference
Cordless (EU) FDA UDI
Description
Del Sol Red Cordless LED Light for EU/CE only FDA UDI

Identifiers

Catalog Number
70393-01 FDA UDI
Primary DI / UDI-DI
00850043007340 FDA UDI
510(k) Number
K072399 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Cosmetic red-light phototherapy system, professional 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

No

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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cosmetic red-light phototherapy system, professional

Del Sol Red Light Therapy System by Hydrafacial LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cosmetic red-light phototherapy system, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hydrafacial LLC

Sources (1)

  • FDA UDI 902fff92-3ccf-4592-80b6-8f191efb2240 36 fields · synced May 30, 2026