XEROSGUARD INC.

FDA Device Registration & Listing · Winnipeg Manitoba, CA · Registration 3023789889

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
3023789889
FEI Number
3023789889
Entity Name
XEROSGUARD INC.
City/State/Country
Winnipeg Manitoba, CA
Establishment Address
30th Floor, 360 Main Street, C/O MLT Aikins LLP, Winnipeg Manitoba R3N 0P5, CA
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Xerosguard Inc. (Owner Number: 10091548)
Owner / Operator Contact Address
30th Floor, 360 Main Street, C/O MLT Aikins LLP, Winnipeg, CA-MB R3N 0P5, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Xerosguard

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EIG Retractor, All Types Dental Class 1 872.4565 2024-10-14

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp. Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Xerosguard Inc.
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 3023789889. Last updated year: 2026. Please use registration number 3023789889 when referencing this establishment in official correspondence.
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