LEMER PAX AMERICA

FDA Device Registration & Listing · Montreal Quebec, CA · Registration 3029900933

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3029900933
FEI Number
3029900933
Entity Name
LEMER PAX AMERICA
City/State/Country
Montreal Quebec, CA
Establishment Address
McGill, Suite 710, Montreal Quebec H2Y 2H4, CA
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Lemer Pax America (Owner Number: 10088691)
Owner / Operator Contact Address
McGill, Suite 710, Montreal, CA-QC H2Y 2H4, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Radshield screen LMP2 Theranojet Theranojet ARA Mediclic Easyview Easysqueeze

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KPY Shield, Protective, Personnel Radiology Class 1 892.6500 2023-12-08
IWR Holder, Syringe, Lead Radiology Class 1 892.6500 2026-05-21

Official Correspondent

No official correspondent registered.

US Agent Details

Yong Sun Business: Emergo Global Representation LLC Email: USAgent@ul.com Phone: (512) 3279997

Related Public Records

Same Entity

Lemer Pax America
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 3029900933. Last updated year: 2026. Please use registration number 3029900933 when referencing this establishment in official correspondence.
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