AGM orthopaedics
LV-MF-000044288 · Latvia · Riga
AGM orthopaedics is registered in the European database on medical devices as a manufacturer, with 58 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 58 |
|---|
Most frequent device types declared: 500HLBK01N, SPAO.
Devices declared under this manufacturer
- Acupressure Octopus High Lumbar orthosis
- Acupressure Octopus High lumbar orthosis
- Acupressure Octopus Lumbosacral orthosis
- Acupressure Octopus Thoracic-shoulder orthosis
- TRUST
- TRUST - Tactical rapid use tourniquet, Gen2, Rescue orange
- TRUST - Tactical rapid use tourniquet, Gen2, Tactical black
- TRUST - Tactical rapid use tourniquet, Gen2, Training blue
Showing 12 of 58 declared devices.
Catalogue references include 100HL0105L, 100HL0205L, 100HL0207L, 100LS0107N, 100LS0202N, 100TC0203N.
European nomenclature codes declared: Y060306, Y060308, Y060307, V9003.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 58 |
| Country of registration | Latvia |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 58 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. AGM orthopaedics was not found in either the U.S. or the Canadian register.