DSSM AG
LI-MF-000017682 · Liechtenstein · Schaan
DSSM AG is registered in the European database on medical devices as a manufacturer, with 98 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 59 |
|---|---|
| Class IIa | 39 |
Among these devices, 94 are declared implantable.
Devices declared under this manufacturer
- PressCeramic HT A3 (4)
- PressCeramic HT A4 (4)
- PressCeramic HT BL4 (4)
- PressCeramic LT A3 (4)
- PressCeramic LT A3.5 (4)
- PressCeramic LT B4 (4)
- PressCeramic LT D4 (4)
- PressCeramic MT A3 (4)
- PressCeramic Opal 2 (4)
- Sagemax Paint 3D Effect Peach 4g
- Sagemax Paint 3D Enamel Cloud 4g
- Sagemax Paint 3D Enamel Shadow 4g
Showing 12 of 98 declared devices.
Catalogue references include 753568, 753585, 753588, 753604, 753610, 753624.
European nomenclature codes declared: P01020101, Q010699, Q019002.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | DSSM AG (LI) · FDA 3034244245 |
| Devices in EUDAMED | 98 |
| Country of registration | Liechtenstein |
Device-level evidence
| Devices with a numeric GTIN | 98 |
|---|---|
| Found in the U.S. device database | 39 |
| Share | 39.8 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | DSSM AG |
What it holds in Canada
| Licences on record | 2 |
|---|---|
| Currently active | 0 |
| Class 3 devices | 2 |
| First licensed | 2025-07-17 |
Licence types: Device Family (1), System (1).
Licensed under: PRESSCERAMIC, SAGEMAX PAINT 3D.
North American profile: Both markets. DSSM AG is registered in both the United States and Canada.