Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042970900

FEI Number

3042970900

Entity Name

XPLR LTD.

City/State/Country

Yehud Tel Aviv, IL

Establishment Address

Ben ami 6 st, Yehud Tel Aviv 5647867, IL

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

XPLR Ltd. (Owner Number: 10094734)

Owner / Operator Contact Address

Ben ami 6 st, Yehud, IL-TA 5647867, IL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K250125

PMA Number

N/A

All Registered Proprietary Names

LMNT O2

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OHS	Light Based Over The Counter Wrinkle Reduction	General, Plastic Surgery	Class 2	878.4810	2025-12-18
OLP	Over-The-Counter Powered Light Based Laser For Acne	General, Plastic Surgery	Class 2	878.4810	2025-12-18

Official Correspondent

Meital Izhaki

US Agent Details

Mark Gordon Email: Mark.W.Gordon@outlook.com Phone: (571) 4072862

Related Public Records

Same Entity

XPLR Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042970900. Last updated year: 2026. Please use registration number 3042970900 when referencing this establishment in official correspondence.