Results for “PEEK Temporary Abutment”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 41 FDA 510(k) incl. De Novo 1 FDA PMA GUDID 35

Country / market European Union (all) 41 United States 36

More countries (5)

Ireland 20 Germany 14 Greece 3 Belgium 2 Italy 2

Risk class Class I Class IIa 26 Class IIb 15 Class III Class II (US) 34

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

75 devices foundsorted by relevance

Clear all

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

PEEK Temporary Abutment

OsteoCare Implant System Limited,United Kingdom Group of variants

Withdrawn Regimes: CE MDD, withdrawn Registry: EUDAMED Class:IIa
SLH DC Temporary PEEK Abutment Hex

SLH Microtech GmbH,Germany

Active Regimes: CE MDR CE MDD Registry: EUDAMED Class:IIb

Previous Next

Showing 61-75 of 75

deviCERTS Global Medical Device Regulatory Database

About [email protected]

Results for “PEEK Temporary Abutment”

Category (EMDN)

PEEK Temporary Abutment

SLH DC Temporary PEEK Abutment Hex