KLE - BEUDAMED

BEUDAMED

⌘K

API Documentation Get API Key Sign in By OpenRegulatory ↗

741 results · 22ms · Sources: EU EUDAMED, US FDA

Filters Classification: FDA Class 2 ×

Filter by

FDA 510(k) 738 FDA classification 3 + More Filters

Country

United States 597 Germany 33 Canada 15 South Korea 14 Switzerland 12 China 11 Japan 11 Taiwan 9 United Kingdom 9 Italy 8 Israel 7 Liechtenstein 2 Netherlands 2 Australia 1 Brazil 1 France 1 Greece 1 Hong Kong 1 India 1 Kenya 1 + More Countries

Classification

FDA Class 2 741 + More Classifications

FDA FEI Number

3006066614 592 3026297922 592 3011824442 591 3012494290 435 3012421607 431 3011689956 421 2110898 420 2511556 417 3010419931 415 3001746544 414 2183301 413 2523320 413 3000719964 413 3003120666 413 3010862763 413 1000118628 412 1000127002 412 1000231788 412 1000272892 412 1013257 412 + More FDA FEI Numbers

Regulation

Us FDA 741 + More Regulations

FDA Registration Number

3006066614 592 3026297922 592 3011824442 591 3012494290 435 3012421607 431 3011689956 421 2110898 420 2511556 416 2437780 415 3010419931 415 2086043 414 2024980 413 2183301 413 2424472 413 3003120666 413 3010864832 413 1000118628 412 1000272892 412 1013257 412 1032227 412 + More FDA Registration Numbers

FDA K Number

K000189 1 K000954 1 K001494 1 K001914 1 K002502 1 K003011 1 K003153 1 K003293 1 K010415 1 K010547 1 K011167 1 K011490 1 K012082 1 K012322 1 K012432 1 K012436 1 K012440 1 K012442 1 K012729 1 K012730 1 + More FDA K Numbers

Implant, Subperiosteal

FDA classification

FDA Class 2 ·Implant, Subperiosteal

<1 …34 35 36 37 38 >

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

BEUDAMED

A better medical device search engine by OpenRegulatory.

API Documentation
API Dashboard
EUDAMED API on GitHub
Imprint

BEUDAMED

Rationale
MDR Notified Bodies
MDR Competent Authorities

OpenRegulatory

OpenRegulatory
Formwork eQMS Software
Digital Health Jobs
EUDAMED Budget Monitor
eidel.io

Tools

510(k) Predicate Finder
Product Code Directory
510(k) Review Times
21 CFR Regulations
NB Comparison

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.

© 2026 OpenReg GmbH. All rights reserved.