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Data / Medical devices / Handle, Scalpel / France

FDA-registered makers of Handle, Scalpel in France: 8 establishments

8 establishments in France are registered with the FDA to make Handle, Scalpel (product code GDZ). 0 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
Handle, Scalpel
Product code
GDZ
Country
France

Makers of Handle, Scalpel in France

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
CF PlastiquesPUSIGNAN Rhone, FranceContract manufacturer0000api.fda.gov
In'tech Medical SASRANG DU FLIERS Pas-de-Calais, FranceContract manufacturer, Exporter to the US0000api.fda.gov
Integra Microfrance SASSAINT AUBIN LE MONIAL Auvergne-Rhone-Alpes, FranceManufacturer, Repackager or relabeler0000api.fda.gov
In2Bones SASSaint-Priest Rhone, FranceExporter to the US, Specification developer0000api.fda.gov
Moria S.A.MASSY Hauts-de-Seine, FranceSpecification developer0000api.fda.gov
Moria S.ABourbon l'Archambault Allier, FranceContract manufacturer0000api.fda.gov
Newclip Technics SASHAUTE GOULAINE Loire-Atlantique, FranceManufacturer, Specification developer0000api.fda.gov
VCN TechnologiesSAINT-PRIEST Auvergne-Rhone-Alpes, 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.