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Data / Medical devices / Canada / 10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies

10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies: FDA-registered device maker in Winnipeg Manitoba, Canada, 15 PMA approvals

10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies is registered with the FDA (registration 3043624366) in Winnipeg Manitoba, Canada. It lists 4 device types. The FDA files 15 PMA approvals under its listings, the newest dated October 19, 2017. Registered through 2026. FDA data exported November 3, 2026.

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Get makers like this oneWatch 10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies
FDA registration number
3043624366
Address
26-360 Keewatin St., Winnipeg Manitoba, Canada, R2X 2R9
Owner or operator
10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies (10095200)
Roles
Exporter to the US, Repackager or relabeler
First device listed
February 4, 2026
Registered through
2026
Brand names listed
Acid, hyaluronic, intraarticular, Implant, dermal, for aesthetic use

Devices it lists

DeviceProduct codeClassRoleSource
Acid, Hyaluronic, IntraarticularMOZ3Exporter to the US, Repackager or relabeleraccessdata.fda.gov
Implant, Dermal, For Aesthetic UseLMH3Exporter to the US, Repackager or relabeleraccessdata.fda.gov
Implant, Dermal, For Aesthetic Use In The HandsPKY3Exporter to the US, Repackager or relabeleraccessdata.fda.gov
Sealant, DuralNQR3Exporter to the US, Repackager or relabeleraccessdata.fda.gov

PMA approvals

Premarket approvals this establishment lists, with the supplements the FDA has decided since.

ApprovedPMA numberDeviceProduct codeSupplementsLatest decisionSource
October 19, 2017P170002RHA 2, RHA 3, RHA 4LMH55August 31, 2026accessdata.fda.gov
August 29, 2017P170007DUROLANEMOZ15December 23, 2025accessdata.fda.gov
August 28, 2015P150010HYMOVISMOZ5April 9, 2025accessdata.fda.gov
February 25, 2014P090031MONOVISCMOZ15August 8, 2023accessdata.fda.gov
October 22, 2013P110033JUVEDERM VOLUMA XCLMH97August 28, 2026accessdata.fda.gov
November 14, 2011P090016BELOTERO BALANCELMH60May 3, 2026accessdata.fda.gov
December 22, 2006P050052RADIESSE INJECTABLE IMPLANTLMH169June 26, 2026accessdata.fda.gov
June 2, 2006P050047JUVEDERM 24HV, JUVEDERM 30 AND JUVEDERM 30HV GEL IMPLANTSLMH101August 28, 2026accessdata.fda.gov
April 7, 2005P040034DURASEAL DURAL SEALANT SYSTEMNQR38February 27, 2026accessdata.fda.gov
December 3, 2004P010029EUFLEXXA (1% SODIUM HYALURONATE)MOZ40September 2, 2026accessdata.fda.gov
August 3, 2004P030050SCULPTRA AND SCULPTRA AESTHETICLMH54September 17, 2026accessdata.fda.gov
February 4, 2004P030019ORTHOVISC HIGH MOLECULAR WEIGHT HYALURONANMOZ23August 28, 2026accessdata.fda.gov
December 12, 2003P020023RESTYLANE INJECTABLE GELLMH12October 21, 2005accessdata.fda.gov
January 24, 2001P980044SUPARTZ FXMOZ62September 4, 2026accessdata.fda.gov
May 28, 1997P950027HYALGAN(R)MOZ15June 28, 2024accessdata.fda.gov

Compare with other makers

Updated August 31, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.