Manufacturer registered with FDA

Dexta Corporation

Napa, CA, United States. Lists 2 dental device types with FDA across 1 registered establishment.

FDA owner/operator2916273Manufacturer
Device types listed
2
Brands and models
0
510(k) clearances
0as applicant
Markets registered in
48 registrations outside the US
Establishments
1United States

Registered in 4 markets

Where regulators' registries name Dexta Corporation as the manufacturer or the registration holder of a device.

All markets
United States: 2 device types listedSouth Korea: 5 registrationsIsrael: 2 registrationsAustralia: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerDexta Corporation2 device types—Below
South KoreaMFDSManufacturerDEXTA CORPORATIONDEXTA Corporation · Dexta Corporation52000–2011Pure Global AI
IsraelAMARManufacturerDEXTA CORPORATIONDexta Corporation2—Pure Global AI
AustraliaTGAManufacturerDexta Corporation12025–2025Pure 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 Dexta Corporation currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Dental Operating LightEAZ · Class 1Dental operating lightsMaker—2014
Dental Chair without Operative UnitNRU · Class 1Dental chairs & operative unitsMaker—2014

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
DEXTA CORP.FDA reg. 2916273NAPA, CA, United StatesManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 2916273). 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.