Not currently registered with FDA under this name

Neirynck & Vogt NV

Pickerington, OH, United States. Named as applicant on 5 dental 510(k) clearances between 2002 and 2002. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
52002–2002
Markets registered in
21 registrations outside the US
Establishments
0—
2002: 5200020102020

510(k) clearances per year, 2000–2026

Registered in 2 markets

Where regulators' registries name Neirynck & Vogt NV as the manufacturer or the registration holder of a device.

All markets
United States: 5 clearancesSouth Korea: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantNeirynck & Vogt NV5 clearances2002–2002Below
South KoreaMFDSManufacturerNeirynck & Vogt n.v.12010–2010Pure 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 Neirynck & Vogt NV as the applicant.

Decided510(k)DeviceDevice type
13 Dec 2002K023477BIOLOYEJH Base Metal Alloy
1 Aug 2002K021971CERALOYEJH Base Metal Alloy
30 Jul 2002K021969CHROLOYEJH Base Metal Alloy
26 Jul 2002K021968CERALOY SOLDEREJH Base Metal Alloy
26 Jul 2002K021965CHROLOY SOLDEREJH Base Metal Alloy

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.