Data / Medical devices / Liechtenstein / DSSM AG
DSSM AG: FDA-registered device maker in Schaan, Liechtenstein, 5 510(k) clearances
DSSM AG is registered with the FDA (registration 3034244245) in Schaan, Liechtenstein. It lists 2 device types. The FDA files 5 510(k) clearances under its listings, the newest dated December 16, 2015. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3034244245
- Address
- Im alten Riet 9, Schaan, Liechtenstein, 9494
- Owner or operator
- IVOCLAR VIVADENT (8010208)
- Roles
- Complaint file establishment
- First device listed
- November 15, 2007
- Registered through
- 2027
- Brand names listed
- IPS Ivocolor, IPS Ivocolor Intro Kit, IPS e.max CAD Cryst Glaze Paste Fluo, IPS e.max Ceram Art, IPS e.max Press, IPS e.max Press HO, IPS e.max Press HT, IPS e.max Press LT and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Retractor, Dental | EIF | 1 | Complaint file establishment | accessdata.fda.gov |
| Powder, Porcelain | EIH | 2 | Complaint file establishment | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 16, 2015 | K152118 | Zenostar MT, Zenostar Color Liquids | EIH | Substantially Equivalent | Wieland Dental + Technik GmbH & Co. KG | accessdata.fda.gov |
| October 29, 2015 | K151894 | IPS Ivocolor | EIH | Substantially Equivalent | Ivoclar Vivadent, AG | accessdata.fda.gov |
| January 5, 2015 | K142233 | zenostar MO, Zenostar T, Zenostar VisualiZr | EIH | Substantially Equivalent | Wieland Dental + Technik GmbH & Co. KG | accessdata.fda.gov |
| June 25, 2012 | K120134 | IPS E.MAX PRESS MULTI | EIH | Substantially Equivalent | Ivoclar Vivadent, AG | accessdata.fda.gov |
| September 8, 1998 | K982616 | IPS EMPRESS 2 | EIH | Substantially Equivalent | Ivoclar North America, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 16, 2015. 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.