Data / Medical devices / Intraoral Camera

Intraoral Camera (QJK): 18 FDA-registered makers in 9 countries

Name: FDA-registered makers of Intraoral Camera
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

18 establishments in 9 countries are registered with the FDA to make Intraoral Camera (product code QJK, Class 2, 21 CFR 872.3661). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code: QJK
Device class: 2
Regulation: 872.3661
Medical specialty: Dental

Makers by country

Country	Makers
China	6
South Korea	3
Mexico	2
Canada	2
Taiwan	1
Israel	1
Brazil	1
United States	1
Thailand	1

Makers of Intraoral Camera

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Maker	Location	Role	Source
Acme Tooling Technology Co., Ltd.	Fuxing Township Changhua, Taiwan	Manufacturer	api.fda.gov
Align Technology, Ltd.	Petach Tikva Central, Israel	Manufacturer	api.fda.gov
Aligntech de Mexico S, de R. L. de C. V.	Cd. Juarez Chihuahua, Mexico	Manufacturer	api.fda.gov
Aligntech de Mexico S, de R. L. de C. V.	Cd. Juarez Chihuahua, Mexico	Manufacturer	api.fda.gov
Alliage S/A Industrias Medico Odontologica	Ribeirao Preto Sao Paulo, Brazil	Manufacturer	api.fda.gov
Beyes Dental Inc	Toronto Ontario, Canada	Manufacturer	api.fda.gov
Clear Capture, LCC	Berkeley Lake, GA, United States	Specification developer	api.fda.gov
DSM Holdings Co., Ltd	Seoul, South Korea	Manufacturer	api.fda.gov
Dongguan Yipincheng Technology Co., Ltd.	Dongguan Guangdong, China	Manufacturer	api.fda.gov
Fabrinet Co., Ltd.	Sriracha Chon Buri, Thailand	Contract manufacturer	api.fda.gov
Guangdong Jinme Medical Technology Co., Ltd.	Foshan Guangdong, China	Manufacturer	api.fda.gov
Huizhou Videya Technology Co., Ltd.	Huizhou Guangdong, China	Manufacturer	api.fda.gov
Ningbo Runyes Medical Instrument Co., Ltd.	Ningbo Zhejiang, China	Complaint file establishment, Contract manufacturer, Manufacturer	api.fda.gov
One Day Dental Partner	Suncheon-si Jeonnam, South Korea	Exporter to the US, Manufacturer	api.fda.gov
Onvet Medical Canada Inc	TORONTO Ontario, Canada	Manufacturer	api.fda.gov
Osstem Implant Co., Ltd.	Gangseo-gu Seoul, South Korea	Specification developer	api.fda.gov
Shenzhen Besdata Technology Co.,ltd	Shenzhen Guangdong, China	Manufacturer	api.fda.gov
Shenzhen Xiazhifeng Electronic Co., Ltd	Shenzhen Guangdong, China	Contract manufacturer, Exporter to the US, Manufacturer	api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.