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Data / Medical devices / Elevator / Switzerland

FDA-registered makers of Elevator in Switzerland: 5 establishments

5 establishments in Switzerland are registered with the FDA to make Elevator (product code HTE). 0 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Elevator
Product code
HTE
Country
Switzerland

Makers of Elevator in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Jabil Switzerland Manufacturing GmbH (Hagendorf)Hagendorf Solothurn, SwitzerlandContract manufacturer0000api.fda.gov
Medos International SarlLe Locle Neuchatel, SwitzerlandSpecification developer0000api.fda.gov
STRYKER GmbHSELZACH Solothurn, SwitzerlandManufacturer0000api.fda.gov
Synthes GMBHZuchwil Solothurn, SwitzerlandSpecification developer0000api.fda.gov
Ulrich AGST. GALLEN Sankt Gallen, 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.