10122110 MANITOBA LTD. O/A FORT GARRY MEDICAL SUPPLIES

FDA Device Registration & Listing · Winnipeg Manitoba, CA · Registration 3043624366

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
3043624366
FEI Number
3043624366
Entity Name
10122110 MANITOBA LTD. O/A FORT GARRY MEDICAL SUPPLIES
City/State/Country
Winnipeg Manitoba, CA
Establishment Address
26-360 Keewatin St., Winnipeg Manitoba R2X 2R9, CA
Establishment Type(s)
Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies (Owner Number: 10095200)
Owner / Operator Contact Address
26-360 Keewatin St., Winnipeg, CA-MB R2X 2R9, CA
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P050047

All Registered Proprietary Names

Acid, hyaluronic, intraarticular Acid, hyaluronic, intraarticular Acid, hyaluronic, intraarticular Acid, hyaluronic, intraarticular Implant, dermal, for aesthetic use Implant, dermal, for aesthetic use Acid, hyaluronic, intraarticular Acid, hyaluronic, intraarticular Acid, hyaluronic, intraarticular Implant, dermal, for aesthetic use Implant, dermal, for aesthetic use Implant, dermal, for aesthetic use

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2026-02-04
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2026-02-04
NQR Sealant, Dural Unknown Class 3 N/A 2026-02-04
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2026-02-04
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2026-02-04
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2026-02-04
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2026-02-04
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2026-02-04
MOZ Acid, Hyaluronic, Intraarticular Unknown Class 3 N/A 2026-02-04
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2026-02-04
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2026-02-04
LMH Implant, Dermal, For Aesthetic Use Unknown Class 3 N/A 2026-02-04

Official Correspondent

Gordon Chubey

US Agent Details

Larry Ordet Business: FDA Solutions Group, LLC Email: info@fdasolutionsgroup.com Phone: (305) 7023161

Related Public Records

Same Entity

10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies
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 3043624366. Last updated year: 2026. Please use registration number 3043624366 when referencing this establishment in official correspondence.
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