Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “FUTURE KNEE 1, P/S Tibial Insert”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED FDA 510(k) incl. De Novo FDA PMA GUDID

Country / market European Union (all) United States

More countries (18)

Germany Italy Türkiye France Spain Netherlands Poland Austria Belgium Ireland Czechia Portugal Greece Sweden Denmark Hungary Romania Northern Ireland

Risk class Class I Class IIa Class IIb Class III Class II (US)

More classes (11)

Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

Verified Verified only

Category (EMDN)

Browse by category

440 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

FUTURE KNEE 1, P/S Tibial Insert

Biotech GmbH,Germany Group of variants

Active Regimes: CE MDD Registry: EUDAMED Class:III
FUTURE KNEE 1, Primary Tibial Insert

Biotech GmbH,Germany Group of variants

Active Regimes: CE MDD Registry: EUDAMED Class:III
FUTURE KNEE 1 Rotating P/S Tibial Insert

Biotech GmbH,Germany Group of variants

Active Regimes: CE MDD Registry: EUDAMED Class:III

Previous Next

Showing 1-20 of 440

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site