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Data / Medical devices / Appliance, Fixation, Spinal Interlaminal / France

FDA-registered makers of Appliance, Fixation, Spinal Interlaminal in France: 25 establishments

25 establishments in France are registered with the FDA to make Appliance, Fixation, Spinal Interlaminal (product code KWP). 3 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 FranceWatch these makers
Device
Appliance, Fixation, Spinal Interlaminal
Product code
KWP
Country
France

Makers of Appliance, Fixation, Spinal Interlaminal in France

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Spinevision SASAntony Hauts-de-Seine, FranceComplaint file establishment, Manufacturer2August 1, 2002000api.fda.gov
LDR MedicalSainte-Savine Aube, FranceSpecification developer1August 8, 2007000api.fda.gov
Microtec SASSerres Castet Pyrenees-Atlantiques, FranceManufacturer1January 15, 2015000api.fda.gov
A.F.T. MicromecaniqueFillinges Haute-Savoie, FranceContract manufacturer0000api.fda.gov
Alpes CN SASReignier-Esery Haute-Savoie, FranceContract manufacturer, Manufacturer0000api.fda.gov
AnthogyrSALLANCHES Haute-Savoie, FranceContract manufacturer0000api.fda.gov
CefimecaLa Talaudiere Loire, FranceContract manufacturer0000api.fda.gov
Clariance-SasBEAURAINS Hauts-de-France, FranceContract manufacturer0000api.fda.gov
Coulot DecolletageCHATELLERAULT Vienne, FranceContract manufacturer0000api.fda.gov
Cousin BiotechWERVICQ-SUD Nord, FranceContract manufacturer0000api.fda.gov
Decomicro SASNaintre Nouvelle-Aquitaine, FranceContract manufacturer0000api.fda.gov
Euclide CareAixe Sur Vienne Haute-Vienne, FranceContract manufacturer0000api.fda.gov
ImplanetMartillac Nouvelle-Aquitaine, FranceManufacturer0000api.fda.gov
Lopitz ManufacturingGradignan Nouvelle-Aquitaine, FranceContract manufacturer0000api.fda.gov
Medicrea InternationalRILLIEUX-LA-PAPE Auvergne-Rhone-Alpes, FranceManufacturer0020api.fda.gov
Oury-Guye & FilsNOGENT Haute-Marne, FranceContract manufacturer0000api.fda.gov
Phen'x TechnologiesChassieu Auvergne-Rhone-Alpes, FranceContract manufacturer0000api.fda.gov
S.M.A.I.OSAINT-PRIEST Auvergne-Rhone-Alpes, FranceManufacturer, Specification developer0000api.fda.gov
Safe Orthopaedics SASFleurieux-Sur-L'Arbresle Rhone, FranceManufacturer0000api.fda.gov
Selenium Medical S.A.S.La Rochelle Charente-Maritime, FranceContract manufacturer0000api.fda.gov
SimagecROUSSET CEDEX Bouches-du-Rhone, FranceContract manufacturer0000api.fda.gov
Simon SASBayeux Calvados, FranceContract manufacturer0000api.fda.gov
Stryker SpineCESTAS Nouvelle-Aquitaine, FranceContract manufacturer0000api.fda.gov
Symmetry Medical Polyvac SASWAMBRECHIES Nord, FranceContract manufacturer0000api.fda.gov
Safe MedicalFleurieux-Sur-L'Arbresle Rhone, FranceContract 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.