Not currently registered with FDA under this name

Harvest Technologies, Corp.

Plymouth, MA, United States. Named as applicant on 1 dental 510(k) clearance between 2001 and 2001. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
12001–2001
Markets registered in
820 registrations outside the US
Establishments
0—
2001: 1200020102020

510(k) clearances per year, 2000–2026

Registered in 8 markets

Where regulators' registries name Harvest Technologies, Corp. as the manufacturer or the registration holder of a device.

All markets
United States: 1 clearancesCanada: 6 registrationsTaiwan: 5 registrationsSouth Korea: 4 registrationsIsrael: 2 registrationsColombia: 1 registrationsPeru: 1 registrationsSaudi Arabia: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantHarvest Technologies, Corp.1 clearances2001–2001Below
CanadaHealth CanadaRegistration holderHARVEST TECHNOLOGIES CORP.61999–1999Pure Global AI
TaiwanTFDAManufacturerHARVEST TECHNOLOGIES CORPORATIONHARVEST TECHNOLOGIES, CORP.52011–2015Pure Global AI
South KoreaMFDSManufacturerHarvest Technologies CorpHarvest Technologies Corp.42003–2012Pure Global AI
IsraelAMARManufacturerHARVEST TECHNOLOGIES CORPORATIONHarvest Technologies Corp.2—Pure Global AI
ColombiaINVIMAManufacturerHARVEST TECHNOLOGIES CORP.1—Pure Global AI
PeruDIGEMIDManufacturerHARVEST TECHNOLOGIES CORPORATION12013–2013Pure Global AI
Saudi ArabiaSFDAManufacturerHarvest Technologies Corp.1—Pure 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 Harvest Technologies, Corp. as the applicant.

Decided510(k)DeviceDevice type
3 Jul 2001K011032SMARTJET BONE GRAFT LIQUID APPLICATOR (SPRAY TIP), MODEL SK/S, SMARTJET BONE GRAFT LIQUID APPLICATOR (DUAL LUMEN CANNULALYC Synthetic Bone Grafting Material

Some of these clearances are listed with FDA today by another company: Globus Medical Inc (1).

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.