Skip to the page

Data / Medical devices / Component, Traction, Invasive / Switzerland

FDA-registered makers of Component, Traction, Invasive in Switzerland: 8 establishments

8 establishments in Switzerland are registered with the FDA to make Component, Traction, Invasive (product code JEC). 4 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.

Device
Component, Traction, Invasive
Product code
JEC
Country
Switzerland

Makers of Component, Traction, Invasive in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
STRYKER GmbHSELZACH Solothurn, SwitzerlandManufacturer12January 14, 2011010api.fda.gov
Medos International SarlLe Locle Neuchatel, SwitzerlandSpecification developer2December 15, 1999000api.fda.gov
Synthes GMBHZuchwil Solothurn, SwitzerlandSpecification developer1August 24, 2007000api.fda.gov
Synthes GMBHSelzach Solothurn, SwitzerlandManufacturer1August 24, 2007000api.fda.gov
Composites Busch SAPorrentruy Jura, SwitzerlandContract manufacturer0000api.fda.gov
HN And M GMBHDerendingen Solothurn, SwitzerlandContract manufacturer0000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Bettlach)Bettlach Solothurn, SwitzerlandContract manufacturer0000api.fda.gov
Spitrex Orthopedics Switzerland SALe Locle 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.