Not currently registered with FDA under this name

Mis - Implant Technologies , Ltd.

Bar Lev Industrial Park, Israel. Named as applicant on 3 dental 510(k) clearances between 2004 and 2011. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
32004–2011
Markets registered in
512 registrations outside the US
Establishments
0—
2004: 12008: 12011: 1200020102020

510(k) clearances per year, 2000–2026

Registered in 5 markets

Where regulators' registries name Mis - Implant Technologies , Ltd. as the manufacturer or the registration holder of a device.

All markets
United States: 3 clearancesColombia: 6 registrationsSouth Korea: 4 registrationsPeru: 1 registrationsTaiwan: 1 registrations
RegisteredHome: IsraelOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantMis - Implant Technologies , Ltd.3 clearances2004–2011Below
ColombiaINVIMAManufacturerM.I.S. IMPLANT TECHNOLOGIES LTD6—Pure Global AI
South KoreaMFDSManufacturerM.I.S. Implant Technologies LtdM.I.S Implant Technologies Ltd42003–2003Pure Global AI
PeruDIGEMIDManufacturerMIS IMPLANT TECHNOLOGIES LTD.12018–2018Pure Global AI
TaiwanTFDAManufacturerM.I.S. IMPLANT TECHNOLOGIES, LTD.12011–2011Pure Global AI

Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026

510(k) clearances

Clearances on which FDA names Mis - Implant Technologies , Ltd. as the applicant.

Decided510(k)DeviceDevice type
15 Sep 2011K103089SEVEN IMPLANTS; BIOCOM IMPLANTS; LANCE IMPLANTSDZE Root-Form Endosseous Implant
17 Dec 2008K080458MIS CREST WIDENERMQN External Mandibular Fixator and/or Distractor
9 Jun 2004K040807MIS DENTAL IMPLANT SYSTEMDZE Root-Form Endosseous Implant

Some of these clearances are listed with FDA today by another company: Dentsply Sirona, Inc. (2).

Sources

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 of the most recent filing, which can be a US agent.