Data / Medical devices / Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component / Switzerland

FDA-registered makers of Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component in Switzerland: 18 establishments

Name: FDA-registered makers of Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component in Switzerland
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

18 establishments in Switzerland are registered with the FDA to make Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component (product code KTT). 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.

Get makers of this device in Switzerland Watch these makers

Device: Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Product code: KTT
Country: Switzerland

Makers of Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component in Switzerland

Maker	Location	Role	510(k) clearances	Latest clearance	Recall events	Source
Synthes GMBH	Zuchwil Solothurn, Switzerland	Specification developer	35	June 11, 2026	0	api.fda.gov
STRYKER GmbH	SELZACH Solothurn, Switzerland	Complaint file establishment, Manufacturer, Specification developer	31	December 19, 2025	6	api.fda.gov
Synthes GMBH	Selzach Solothurn, Switzerland	Exporter to the US, Manufacturer	19	June 11, 2026	0	api.fda.gov
Gexfix SA	Le Grand-Saconnex Geneve, Switzerland	Manufacturer	2	December 28, 2016	0	api.fda.gov
Composites Busch SA	Porrentruy Jura, Switzerland	Contract manufacturer	0		0	api.fda.gov
Frueh Verpackungstechnik AG	Fehraltorf Zurich, Switzerland	Contract manufacturer	0		0	api.fda.gov
HN And M GMBH	Derendingen Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Balsthal)	Balsthal Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Bettlach)	Bettlach Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Grenchen)	Grenchen Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Hagendorf)	Hagendorf Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Mezzovico)	Mezzovico Ticino, Switzerland	Contract manufacturer	0		0	api.fda.gov
Jabil Switzerland Manufacturing GmbH (Raron)	Raron Valais, Switzerland	Contract manufacturer	0		0	api.fda.gov
Mawatec AG	Selzach Solothurn, Switzerland	Contract manufacturer	0		0	api.fda.gov
Medartis AG	BASEL Basel-Stadt, Switzerland	Manufacturer	0		0	api.fda.gov
Moser-Baer AG	Sumiswald Bern, Switzerland	Contract manufacturer	0		0	api.fda.gov
Smith & Nephew Orthopaedics AG	AARAU Aargau, Switzerland	Manufacturer	0		0	api.fda.gov
Spitrex Orthopedics Switzerland SA	Le Locle Neuchatel, Switzerland	Contract manufacturer	0		0	api.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.