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Data / Medical devices / External Mandibular Fixator And/Or Distractor / Switzerland

FDA-registered makers of External Mandibular Fixator And/Or Distractor in Switzerland: 7 establishments

7 establishments in Switzerland are registered with the FDA to make External Mandibular Fixator And/Or Distractor (product code MQN). 3 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
External Mandibular Fixator And/Or Distractor
Product code
MQN
Country
Switzerland

Makers of External Mandibular Fixator And/Or Distractor in Switzerland

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Synthes GMBHZuchwil Solothurn, SwitzerlandSpecification developer12May 8, 2017000api.fda.gov
Synthes GMBHSelzach Solothurn, SwitzerlandManufacturer6August 23, 2012000api.fda.gov
Medartis AGBASEL Basel-Stadt, SwitzerlandManufacturer1August 22, 2005000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Balsthal)Balsthal Solothurn, SwitzerlandContract manufacturer0000api.fda.gov
Jabil Switzerland Manufacturing GmbH (Bettlach)Bettlach Solothurn, 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

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.