Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “”

Name, manufacturer or identifier

Manufacturer (optional)

Filters1 active

Registry EUDAMED 99 FDA 510(k) 1 FDA PMA GUDID 64

Country / market European Union (all) 92 United States 65

More countries (2)

Spain 60 Germany 32

Risk class Class I 62 Class IIa Class IIb 38 Class III Class II (US) 64

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 Validated only

Category (EMDN)

Browse by category

164 devices foundsorted by relevance

Manufacturer: Zfx GmbH× Clear all

Device · Manufacturer · Authorizations

GenTek® UDI-DI 04251881700466

Zfx GmbH,Germany Class I

Active CE MDR EUDAMEDGUDID I
18 variants
- GenTek® ZFX05Z-ZB-EX-41
- See all variants of this device
Zfx Titanium Screws UDI-DI 04251881702309

Zfx GmbH,Germany Class IIb

Active CE MDR EUDAMED IIb
23 variants
- Zfx Titanium Screws ZFX09-3I-LO-HL
- Zfx Titanium Screws ZFX09-ST-SC
- Zfx Titanium Screws ZFX09-ZI-SW-48-HL
- Zfx Titanium Screws ZFX09-ZI-TA-HL
- Zfx Titanium Screws ZFX09000631
- Zfx Titanium Screws ZFX09000632
- Zfx Titanium Screws ZFX09000637
- Zfx Titanium Screws ZFX09000649
- Zfx Titanium Screws ZFX09002111
- Zfx Titanium Screws ZFX09002323
- See all variants of this device
Zfx® Intraoral Scanbody UDI-DI 04251881761801

Zfx GmbH,Germany Class I

Active CE MDR EUDAMED I
39 variants
- Zfx® Intraoral Scanbody ZFX05002015
- See all variants of this device
GenTek® UDI-DI 04251881713725

Zfx GmbH,Germany Class IIb

Active CE MDR EUDAMED IIb
11 variants
- GenTek® ZFX09-ZB-LP-GTS
- GenTek® ZFX09-ZB-TA-RS
- GenTek® ZFX11-ZB-EX-3447-NEL
- GenTek® ZFX11-ZB-EX-4147-EL
- See all variants of this device

Showing 81-100 of 164

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site