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LS Pro Systems

FDA UDI

Class II (US FDA UDI)

by Wellness Without Limits Llc

Identity

Trade Name
LS Pro Systems FDA UDI
Generic Name
Red/infrared light phototherapy unit FDA UDI
Device Name
LS Pro Systems 3 Port Controller power supply for LS Pro Systems LED therapeutic pad FDA UDI
Model / Reference
XP3 FDA UDI
Description
LS Pro Systems 3 Port Controller power supply for LS Pro Systems LED therapeutic pad FDA UDI

Identifiers

Primary DI / UDI-DI
00850061407016 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Red/infrared light phototherapy unit 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Red/infrared light phototherapy unit

LS Pro Systems by Wellness Without Limits Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Red/infrared light phototherapy unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 83c0ab09-2033-4a21-8f6d-5d902fdf16a6 33 fields · synced May 30, 2026