K021899 - BEUDAMED

BEUDAMED

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401 results · 41ms · Sources: EU EUDAMED, US FDA

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FDA 510(k) 371 FDA registration 24 FDA classification 6 + More Filters

Country

United States 372 Mexico 12 United Kingdom 8 China 3 Canada 2 Argentina 1 Australia 1 Chile 1 Sweden 1 + More Countries

Classification

FDA Class 2 270 FDA Class 1 107 + More Classifications

FDA FEI Number

3012494290 375 6664 374 3006066614 373 3012421607 373 3013557562 373 3026297922 373 1000137528 371 1417592 371 3002897187 371 3003418325 371 3007208013 371 3013298431 371 3026408938 371 3000268902 337 3001124136 337 2183301 335 3001746544 335 3008875470 335 3010605677 335 3010862763 335 + More FDA FEI Numbers

Regulation

Us FDA 401 + More Regulations

FDA Registration Number

3012494290 375 8021899 374 3006066614 373 3012421607 373 3013557562 373 3026297922 373 1417592 371 2435946 371 3003418325 371 3007208013 371 3013298431 371 3026408938 371 9616872 371 3000268902 337 3001124136 337 2024980 335 2183301 335 2437780 335 3010605677 335 3010864832 335 + More FDA Registration Numbers

FDA K Number

Den230068 1 K000211 1 K000269 1 K000355 1 K000357 1 K000436 1 K000502 1 K000530 1 K000598 1 K000677 1 K000715 1 K001108 1 K001136 1 K001360 1 K001435 1 K001444 1 K001518 1 K001577 1 K001623 1 K001649 1 + More FDA K Numbers

Material, Tooth Shade, Resin

FDA classification

FDA Class 2 ·Material, Tooth Shade, Resin

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

BEUDAMED

A better medical device search engine by OpenRegulatory.

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BEUDAMED

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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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