Registered with FDA

Global Dental Transfer Ltd

Beer Sheva, Israel. Lists 4 dental device types with FDA across 1 registered establishment.

FDA owner/operator10074916Repacker / relabeler
Device types listed
4
Brands and models
2
510(k) clearances
0as applicant
Markets registered in
1United States
Establishments
1Israel

Devices listed with FDA

What Global Dental Transfer Ltd currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Root-Form Endosseous ImplantDZE · Class 2Dental implantsLister
Global Dental Transfer Dental Implant System
2020
Endosseous Dental Implant AbutmentNHA · Class 2Implant abutmentsLister
Global Dental Transfer Dental Implant System
2020
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsLister—2025
Non-Irrigation Endosseous Dental Implant Drill BitsQRQ · Class 1Implant instruments & surgical kitsLister—2025

Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026

Also lists devices cleared under other names

Global Dental Transfer Ltd lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.

Original applicants: d.a.n.d metal industries north LTD (1), DSI Dental Solutions Ltd (1).

Decided510(k)DeviceApplicantDevice type
21 Apr 2025K250176DAND Dental Implant Systemd.a.n.d metal industries north LTDDZE Root-Form Endosseous Implant
1 Apr 2020K200188DSI Dental Implant SystemDSI Dental Solutions LtdDZE Root-Form Endosseous Implant

Registered establishments

EstablishmentLocationWhat it does
GLOBAL DENTAL TRANSFER LTDFDA reg. 3017013344Beer Sheva Southern, IsraelRepacker / relabeler

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10074916). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.