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Data / Medical devices / Pin, Fixation, Smooth / Switzerland

FDA-registered makers of Pin, Fixation, Smooth in Switzerland: 13 establishments

13 establishments in Switzerland are registered with the FDA to make Pin, Fixation, Smooth (product code HTY). 6 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Pin, Fixation, Smooth
Product code
HTY
Country
Switzerland

Makers of Pin, Fixation, Smooth in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
STRYKER GmbHSELZACH Solothurn, SwitzerlandComplaint file establishment, Manufacturer, Specification developer7June 20, 2017010api.fda.gov
Medos International SarlLe Locle Neuchatel, SwitzerlandSpecification developer3May 17, 2013000api.fda.gov
Synthes GMBHZuchwil Solothurn, SwitzerlandSpecification developer2July 18, 1997000api.fda.gov
Medartis AGBASEL Basel-Stadt, SwitzerlandManufacturer1September 23, 2009000api.fda.gov
SYNTHES GMBH / Synthes Produktions GmbHOberdorf, Baselland Basel-Landschaft, SwitzerlandSpecification developer1January 9, 2014000api.fda.gov
Synthes GMBHSelzach Solothurn, SwitzerlandManufacturer1April 2, 1997000api.fda.gov
Leitner AGBusswil Bern, SwitzerlandContract manufacturer0000api.fda.gov
Ruetschi Technology AGMuntelier Fribourg, SwitzerlandContract manufacturer0000api.fda.gov
Ruetschi Technology SAYverdon-les-Bains Vaud, SwitzerlandContract manufacturer0000api.fda.gov
Samaplast AGSankt Margrethen Sankt Gallen, SwitzerlandContract manufacturer0000api.fda.gov
Smith & Nephew Orthopaedics AGAARAU Aargau, SwitzerlandManufacturer0000api.fda.gov
Spitrex Orthopedics Switzerland SALe Locle Neuchatel, SwitzerlandContract manufacturer0000api.fda.gov
SURGICAL FUSION TECHNOLOGIES GmbHSchlieren Zurich, SwitzerlandSpecification developer0000api.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.