Askorn Medical
FR-MF-000001716 · France · Cesson-Sévigné
Askorn Medical is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 33 |
|---|
Most frequent device types declared: HIP HOLD VA.
Among these devices, 4 are declared reusable.
Devices declared under this manufacturer
- Adjustable Tibial Resector Ankle Yoke
- Alix Pliers
- CORTTAPE PORTE IMPLANT INCLINE DROIT
- CORTTAPE PORTE IMPLANT INCLINE GAUCHE 40-70mm
- CORTTAPE SLIDER 1
- Ensemble extracteur universel de tige fémorale
- FingerFix Pliers
- Kirofix Ballast
- Kirofix Ring
- Kirofix Small
- Kit de 3 coussins antistatiques cuir
- OSSKAR Kit
Showing 12 of 33 declared devices.
Catalogue references include 0001-00-04, 0001-00-16, 0081-01-00, 0197-00-00, 0208-02-05, 0226-04-00.
European nomenclature codes declared: H9007, V0804, V9099, L0399, P09120499, L091101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ASKORN MEDICAL (FR) · FDA 3008880500 |
| Devices in EUDAMED | 33 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 33 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 3.0 % |
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: United States only. Askorn Medical is registered in the United States but was not found in the Canadian register.