Manufacturer registered with FDA

Endocraft LLC

Newton, MA, United States. Lists 1 dental device type with FDA across 1 registered establishment.

FDA owner/operator9035069Manufacturer
Device types listed
1
Brands and models
1
510(k) clearances
0as applicant
Markets registered in
23 registrations outside the US
Establishments
1United States

Registered in 2 markets

Where regulators' registries name Endocraft LLC as the manufacturer or the registration holder of a device.

All markets
United States: 1 device types listedEuropean Union: 3 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerEndocraft LLC1 device types—Below
European UnionEUDAMEDManufacturerEndocraft LLC3—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

Devices listed with FDA

What Endocraft LLC currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Suction Operatory UnitEBR · Class 1Suction & evacuation unitsMaker
Suction Cannula
2023

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

Registered establishments

EstablishmentLocationWhat it does
ENDOCRAFT LLC.FDA reg. 1225968Newton, MA, United StatesManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 9035069). 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.