Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “K3Pro Titanium base”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 114 FDA 510(k) incl. De Novo FDA PMA GUDID 32

Country / market European Union (all) 114 United States 32

More countries (1)

Germany 114

Risk class Class I Class IIa Class IIb 114 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

114 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

K3Pro Titanium base

Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG,Germany Group of variants

Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:IIb
K3Pro Caps

Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG,Germany Group of variants

Active Regimes: CE MDD Registry: EUDAMEDGUDID Class:IIb

Previous Next

Showing 1-20 of 114

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site