Not currently registered with FDA under this name

Camsight Co., Inc.

Los Angeles, CA, United States. Named as applicant on 4 dental 510(k) clearances between 1999 and 2007. No establishment is registered with FDA under this exact name today.

Device types listed
0
Brands and models
0
510(k) clearances
41999–2007
Markets registered in
33 registrations outside the US
Establishments
0—
1999: 12001: 12006: 12007: 11990200020102020

510(k) clearances per year, 1990–2026

Registered in 3 markets

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

All markets
United States: 4 clearancesTaiwan: 2 registrationsSouth Korea: 1 registrations
RegisteredHome: United StatesOne marker per market
MarketRegulatorNamed asName on the registryRegistrationsIssuedRecords
United StatesFDAApplicantCamsight Co., Inc.4 clearances1999–2007Below
TaiwanTFDAManufacturerCAMSIGHT CO., INC.22006–2011Pure Global AI
South KoreaMFDSManufacturerCamSight Co., Inc.12007–2007Pure 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 Camsight Co., Inc. as the applicant.

Decided510(k)DeviceDevice type
7 Mar 2007K063646OPTIEIA Operative Dental Unit
12 Jan 2006K053221CDMX-HMUH Digital Extraoral Source X-Ray System
21 May 2001K010915CDMXMUH Digital Extraoral Source X-Ray System
19 Jan 1999K983739OPTUM, INTRAORAL CAMERA SYSTEMEIA Operative Dental Unit

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.