Manufacturer registered with FDA

GP Implants Ltd

Netanya, Israel. Lists 2 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.

FDA owner/operator10056706Specification developer

Device types listed: 2
Brands and models: 2
510(k) clearances: 12017–2017
Markets registered in: 1United States
Establishments: 1Israel

510(k) clearances per year, 2007–2026

Devices listed with FDA

What GP Implants Ltd currently lists, by FDA device type, with the brand and model names on the listing.

Device type	Category	Role	Brands and models	Listed since
Root-Form Endosseous ImplantDZE · Class 2	Dental implants	Maker	GP Implant System	2018
Endosseous Dental Implant AbutmentNHA · Class 2	Implant abutments	Maker	GP Implant System	2018

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

510(k) clearances

Clearances on which FDA names GP Implants Ltd as the applicant.

Decided	510(k)	Device	Device type
22 Jun 2017	K162299	Spiral Shape Dental Implant System	DZE Root-Form Endosseous Implant

Registered establishments

Establishment	Location	What it does
GP IMPLANTS LTDFDA reg. 3014270103	Netanya Central, Israel	Specification developer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10056706). 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.