FDA Device Establishments · JSON-LD · Markdown

Kinetec SAS

FEI 3006734242 · Manufacture Medical Device · Status: Active

FEI Number3006734242
Owner / OperatorKinetec USA, Inc. (#10045573)
AddressZone Industrielle de Tournes, Rue Maurice Périn, Tournes Ardennes, F-08090, FR
Mandatory US AgentKinetec USA, Inc.
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)BXB
Regulation § (21 CFR)890.5380
Proprietary namesKinetec 6080; Kinetec USA; Kinetec Spectra XL; Kinetec Spectra; Kinetec Spectra Essential; Kinetec Prima Advance; Kinetec Prima XL; Kinetec Performa; Kinetec Centura B&W; Kinetec Breva

External sources

Source: openFDA. Public-domain (CC0).