Manufacturer registered with FDA

Innovaid Co.

Seoul, South Korea. Lists 3 dental device types with FDA across 1 registered establishment.

FDA owner/operator10087283Manufacturer
Device types listed
3
Brands and models
4
510(k) clearances
0as applicant
Markets registered in
33 registrations outside the US
Establishments
1South Korea

Registered in 3 markets

Where regulators' registries name Innovaid Co. as the manufacturer or the registration holder of a device.

All markets
United States: 3 device types listedAustralia: 2 registrationsSouth Korea: 1 registrations
RegisteredHome: South KoreaOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAManufacturerInnovaid Co.3 device types—Below
AustraliaTGAManufacturerInnovaid Co22026–2026Pure Global AI
South KoreaMFDSManufacturerINNOVAID A/S12017–2017Pure 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 Innovaid Co. currently lists, by FDA device type, with the brand and model names on the listing.

Device typeCategoryRoleBrands and modelsListed since
Posterior with Metal Insert Artificial TeethELJ · Class 1—Maker
Teeth, Artificial, With Metal Insert
2023
Preformed CrownELZ · Class 1—Maker
Dentlink Zirconia Crown
2026
Endosseous Dental Implant AccessoriesNDP · Class 1Implant instruments & surgical kitsMaker
Dentlink Implant Surgical Guide, ResinDentlink Titanium Scan Body
2026

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
INNOVAID CO.FDA reg. 3026400126Seoul, South KoreaManufacturer

Sources

FDA establishment registration & device listing (search FDA, owner/operator 10087283). 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.