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Data / Medical devices / Thoracolumbosacral Pedicle Screw System / Switzerland

FDA-registered makers of Thoracolumbosacral Pedicle Screw System in Switzerland: 22 establishments

22 establishments in Switzerland are registered with the FDA to make Thoracolumbosacral Pedicle Screw System (product code NKB). 10 have a 510(k) clearance or PMA approval on file and 2 have 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
Thoracolumbosacral Pedicle Screw System
Product code
NKB
Country
Switzerland

Makers of Thoracolumbosacral Pedicle Screw System in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Medos International SarlLe Locle Neuchatel, SwitzerlandSpecification developer48October 21, 2025000api.fda.gov
Synthes GMBHSelzach Solothurn, SwitzerlandManufacturer33July 1, 2016000api.fda.gov
Synthes GMBHZuchwil Solothurn, SwitzerlandSpecification developer32March 29, 2017000api.fda.gov
Medacta International SACastel San Pietro Ticino, SwitzerlandComplaint file establishment, Manufacturer12April 28, 2026000api.fda.gov
Medacta International SARancate Ticino, SwitzerlandComplaint file establishment, Manufacturer12April 28, 2026000api.fda.gov
Spineart SAPlan-les-Ouates, SwitzerlandComplaint file establishment, Specification developer7May 1, 2026030api.fda.gov
Icotec AGAltstaetten Sankt Gallen, SwitzerlandComplaint file establishment, Manufacturer4February 27, 2025010api.fda.gov
Neo Medical S.A.Villette (Lavaux) Vaud, SwitzerlandSpecification developer2December 23, 2024000api.fda.gov
Coligne AGZurich, SwitzerlandManufacturer1May 19, 2021000api.fda.gov
Getset Surgical S.A.Epalinges Vaud, SwitzerlandSpecification developer1January 11, 2021000api.fda.gov
Frueh Verpackungstechnik AGFehraltorf Zurich, SwitzerlandContract manufacturer0000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Hagendorf)Hagendorf Solothurn, SwitzerlandContract manufacturer0000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Le Locle)Le Locle Neuchatel, SwitzerlandContract manufacturer0000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Mezzovico)Mezzovico Ticino, SwitzerlandContract manufacturer0000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Raron)Raron Valais, SwitzerlandContract manufacturer0000api.fda.gov
Leitner AGBusswil Bern, SwitzerlandContract manufacturer0000api.fda.gov
Moser-Baer AGSumiswald Bern, SwitzerlandContract manufacturer0000api.fda.gov
Ruetschi Technology AGMuntelier Fribourg, SwitzerlandContract manufacturer0000api.fda.gov
Samaplast AGSankt Margrethen Sankt Gallen, SwitzerlandContract manufacturer0000api.fda.gov
Spitrex Orthopedics Switzerland SALe Locle Neuchatel, SwitzerlandContract manufacturer0000api.fda.gov
SURGICAL FUSION TECHNOLOGIES GmbHSchlieren Zurich, SwitzerlandSpecification developer0000api.fda.gov
Tectri SACourt Bern, 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.