FDA device listing
Implant, dermal, for aesthetic use
FDA device listing 1532559737 · 10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies
Key facts
| Proprietary names | Implant, dermal, for aesthetic use |
|---|---|
| Owner/operator | 10122110 Manitoba Ltd. O/A Fort Garry Medical Supplies |
| Owner/operator number | 10095200 |
| Premarket submissions | P020023 |
| Product codes | LMH |
| Device names | LMH - Implant, Dermal, For Aesthetic Use |
| Device class | Class III |
| Classification regulations (21 CFR) | ORCA1.LMH |
| Review panels | General & Plastic Surgery |
| Registered establishments | 10122110 MANITOBA LTD. O/A FORT GARRY MEDICAL SUPPLIES |
| Establishment registrations | 3043624366 |
| FEI numbers | 3043624366 |
| Establishment operations | Foreign Exporter, Repackager/Relabeler |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database