NEXXT SPINE, LLC - BEUDAMED

BEUDAMED

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21 results · 45ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

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FDA 510(k) 21 + More Filters

Country

United States 21 + More Countries

Classification

FDA Class 2 21 + More Classifications

FDA FEI Number

1000477302 21 1526534 21 2027467 21 3002806315 21 3002806685 21 3002808269 21 3002980729 21 3003120897 21 3003128516 21 3003477135 21 3004142400 21 3004188066 21 3005706667 21 3005819474 21 3007922509 21 3008583793 21 3008599177 21 3009973505 21 3010032903 21 3010047454 21 + More FDA FEI Numbers

Regulation

Us FDA 21 + More Regulations

FDA Registration Number

1030489 21 1226544 21 1526534 21 2027467 21 2031966 21 3003120897 21 3003477135 21 3004142400 21 3004188066 21 3004774118 21 3005706667 21 3005819474 21 3007922509 21 3008583793 21 3009973505 21 3010032903 21 3010047454 21 3010120104 21 3010123206 21 3014655115 21 + More FDA Registration Numbers

Saxxony Posterior Cervical Thoracic System

FDA Class 2 ·Orthopedic

Data last updated 04 / 2026. Visit the official EUDAMED website for up-to-date data.

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EU MDR

EU MDR Medical Devices EU MDR Active Medical Devices EU MDR Class I Medical Devices EU MDR Class I Software Devices EU MDR Class IIa Medical Devices EU MDR Class IIa Software Devices EU MDR Class IIb Medical Devices EU MDR Class IIb Software Devices EU MDR Class III Medical Devices EU MDR Class III Software Devices EU MDR Implantable Medical Devices EU MDR Measuring Function Medical Devices EU MDR Software Medical Devices

EU IVDR

EU IVDR In Vitro Diagnostic Devices EU IVDR Class A In Vitro Diagnostic Devices EU IVDR Class A Software Devices EU IVDR Class B In Vitro Diagnostic Devices EU IVDR Class B Software Devices EU IVDR Class C In Vitro Diagnostic Devices EU IVDR Class C Software Devices EU IVDR Class D In Vitro Diagnostic Devices EU IVDR Class D Software Devices EU IVDR Instrument Devices EU IVDR Kit Devices EU IVDR Reagent Devices EU IVDR Software Devices

FDA

FDA Medical Devices FDA Class I Medical Devices FDA Class II Medical Devices FDA Class III Medical Devices

By Country

EU IVDR Medical Devices from China EU IVDR Medical Devices from France EU IVDR Medical Devices from Germany EU IVDR Medical Devices from Romania EU IVDR Medical Devices from United States EU MDR Medical Devices from China EU MDR Medical Devices from Egypt EU MDR Medical Devices from Finland EU MDR Medical Devices from France EU MDR Medical Devices from Germany EU MDR Medical Devices from Italy EU MDR Medical Devices from Pakistan EU MDR Medical Devices from Poland EU MDR Medical Devices from Spain EU MDR Medical Devices from Türkiye EU MDR Medical Devices from United Kingdom EU MDR Medical Devices from United States

Notified Bodies

BSI Group The Netherlands B.V. DEKRA Certification B.V. DNV Product Assurance AS POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. SGS Belgium NV TÜV Rheinland LGA Products GmbH TÜV SÜD Product Service GmbH UDEM Uluslararasi Belgelendirme Denetim Egitim Merkezi San. ve Tic. A.Ş.

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