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Data / Medical devices / Liechtenstein / Estetic Ceram AG

Estetic Ceram AG: FDA-registered device maker in Triesen, Liechtenstein, 2 510(k) clearances

Estetic Ceram AG is registered with the FDA (registration 3009081830) in Triesen, Liechtenstein. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 5, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3009081830
Address
Landstrasse 109, Postfach 223, Triesen, Liechtenstein, 9495
Owner or operator
estetic ceram ag (10044453)
Roles
Contract manufacturer, Manufacturer
First device listed
June 13, 2013
Registered through
2026
Brand names listed
iNK3D, mµILLUSION, priti perfect

Devices it lists

DeviceProduct codeClassRoleSource
Powder, PorcelainEIH2Contract manufacturer, Manufactureraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 5, 2025K251084zirkon; structure; LFU shades, stains and glazesEIHSubstantially EquivalentEstetic Ceram AGaccessdata.fda.gov
June 5, 2017K163228APVolution SystemEIHSubstantially EquivalentAesthetic-Press, LLCaccessdata.fda.gov

Compare with other makers

Updated June 5, 2025. 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.