FDA.report

Zfx GmbH

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
30089327793008932779Zfx GmbH1N2026-01-01Kopernikusstr. 15 Dachau Bavaria DE 85221

GUDID Contact Samples

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDIDProductPhoneEmail
04251881700220GenTek® Friction-Fit Abutment Removal Tool, Narrow Platform - ZFX02-RTNP1-800-342-5454dentalcs@zimvie.com
04251881700244GenTek® Friction-Fit Abutment Removal Tool, Standard Platform - ZFX02-RTSP1-800-342-5454dentalcs@zimvie.com
04251881700428GenTek® Hexalobular Screwdriver, 21 mm - ZFX02HLD211-800-342-5454dentalcs@zimvie.com
04251881700442GenTek® Hexalobular Screwdriver, 28 mm - ZFX02HLD281-800-342-5454dentalcs@zimvie.com

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
3268931025637253K231915Zfx AbutmentsNHA2024-03-01
3268932014178774

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
NHA12024-03-01

PMN

GUDID

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