Not currently registered with FDA under this name

Chiron Vision Corp.

Horsham, PA, United States. Named as applicant on 2 dental 510(k) clearances between 1992 and 1994. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
21992–1994
Markets registered in
33 registrations outside the US
Establishments
0—
1992: 11994: 11990200020102020

510(k) clearances per year, 1990–2026

Registered in 3 markets

Where regulators' registries name Chiron Vision Corp. as the manufacturer or the registration holder of a device.

All markets
United States: 2 clearancesTaiwan: 2 registrationsSouth Korea: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantChiron Vision Corp.2 clearances1992–1994Below
TaiwanTFDAManufacturerCHIRON VISION CORPORATION21997–1997Pure Global AI
South KoreaMFDSManufacturerCHIRON.VISION CORPORATION11999–1999Pure 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 Chiron Vision Corp. as the applicant.

Decided510(k)DeviceDevice type
25 Jan 1994K932600MODIFIED SITE POWER HANDPIECE IIEKX Ac-Powered Direct Drive Handpiece
23 Jun 1992K922077MODIFIED SITE POWER HANDPIECEEKX Ac-Powered Direct Drive Handpiece

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.