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Data / Medical devices / Implant, Endosseous, Root-Form / Switzerland

FDA-registered makers of Implant, Endosseous, Root-Form in Switzerland: 20 establishments

20 establishments in Switzerland are registered with the FDA to make Implant, Endosseous, Root-Form (product code DZE). 13 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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Device
Implant, Endosseous, Root-Form
Product code
DZE
Country
Switzerland

Makers of Implant, Endosseous, Root-Form in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Institut Straumann AGBASEL Basel-Stadt, SwitzerlandComplaint file establishment, Specification developer53March 10, 2026000api.fda.gov
Straumann Villeret SAVILLERET Bern, SwitzerlandManufacturer50March 10, 2026000api.fda.gov
Nobel Biocare Services AGKloten Zurich, SwitzerlandSpecification developer31February 18, 2026010api.fda.gov
Thommen Medical, AGGRENCHEN Solothurn, SwitzerlandManufacturer7September 29, 2017000api.fda.gov
Z-Systems AGOensingen Solothurn, SwitzerlandManufacturer7December 1, 2020000api.fda.gov
Biodenta Swiss AGBerneck Sankt Gallen, SwitzerlandSpecification developer5June 13, 2014000api.fda.gov
CAMLOG Biotechnologies GmbHBasel Basel-Stadt, SwitzerlandExporter to the US, Specification developer5September 29, 2020000api.fda.gov
Sic Invent AGBasel Town Basel-Landschaft, SwitzerlandExporter to the US, Manufacturer3March 17, 2022000api.fda.gov
Tri Dental Implants Int. AGHuenenberg Zug, SwitzerlandManufacturer3January 8, 2025000api.fda.gov
CeramTec Schweiz GmbHSpreitenbach Aargau, SwitzerlandManufacturer2November 30, 2016000api.fda.gov
SDS Swiss Dental SolutionsKreuzlingen Thurgau, SwitzerlandSpecification developer2February 20, 2020000api.fda.gov
Infinetamed AGSarnen Obwalden, SwitzerlandComplaint file establishment, Manufacturer, Specification developer1November 15, 2024000api.fda.gov
Medartis AGBASEL Basel-Stadt, SwitzerlandManufacturer1October 21, 2005000api.fda.gov
Cendres+metaux SABiel/Bienne Bern, SwitzerlandContract manufacturer0000api.fda.gov
Ceramaret SABOLE Neuchatel, SwitzerlandContract manufacturer0000api.fda.gov
Diener AG Precision MachiningEmbrach Zurich, SwitzerlandContract manufacturer0000api.fda.gov
Frueh Verpackungstechnik AGFehraltorf Zurich, SwitzerlandContract manufacturer, Contract sterilizer0000api.fda.gov
Rickli Micromecanique SAVauffelin Bern, SwitzerlandContract manufacturer0000api.fda.gov
Samaplast AGSankt Margrethen Sankt Gallen, SwitzerlandContract manufacturer0000api.fda.gov
Theia Holding SALa Chaux-de-Fonds Neuchatel, SwitzerlandContract manufacturer0000api.fda.gov

Updated November 2, 2026. 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.