SunPowerLED

GUDID 08500723550063

KERBER USA INC.

Red/infrared light phototherapy unit
Primary Device ID08500723550063
NIH Device Record Key22d65701-f560-4e8b-9f35-d5b489aa6774
Commercial Distribution StatusIn Commercial Distribution
Brand NameSunPowerLED
Version Model NumberCanopy
Company DUNS144906017
Company NameKERBER USA INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108500723550063 [Primary]

FDA Product Code

ILYLamp, Infrared, Therapeutic Heating

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-06
Device Publish Date2026-02-26

On-Brand Devices [SunPowerLED]

08500723550063Canopy
08500723550056Helmet -810
08500723550049Mini-Canopy
08500723550025Palm Professional
08500723550018Palm Ultimate
08500723550001SuperPalm 1050

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