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Onlux

FDA UDI

Class II (US FDA UDI)

by Physiohab Llc

Identity

Trade Name
ONLUX FDA UDI
Generic Name
Blue/red/infrared phototherapy lamp FDA UDI
Device Name
LED Infrared light therapy wrap for the ankle FDA UDI
Model / Reference
OLA3001 FDA UDI
Description
LED Infrared light therapy wrap for the ankle FDA UDI

Identifiers

Primary DI / UDI-DI
00860013229054 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Blue/red/infrared phototherapy lamp 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blue/red/infrared phototherapy lamp

Onlux by Physiohab Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blue/red/infrared phototherapy lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Physiohab Llc

Sources (1)

  • FDA UDI 7b83c545-c67d-40e0-a6ae-90e2da05b889 33 fields · synced May 30, 2026