Camsight Co., Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Camsight Co., Inc. makes
Camsight Co., Inc. manufactures the CDMX-H, a Class I medical device, and the OPTI and CDMX, both Class II devices. These products appear to include optical and imaging solutions, likely for diagnostic or procedural guidance applications in clinical settings.
The company’s portfolio is regulated under the FDA’s 510(k) pathway, with devices classified as Class I and Class II. Their products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Cdmx-H Ref K053221
Regimes: 510(k) Registry: 510(k)Opti Ref K063646
Regimes: 510(k) Registry: 510(k)Optum, Intraoral Camera System Ref K983739
Regimes: 510(k) Registry: 510(k)Cdmx Ref K010915
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Camsight Co., Inc. have in the registry?
The registry currently lists 4 devices for Camsight Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Camsight Co., Inc.'s devices?
Among its 4 most recently registered devices, Camsight Co., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Camsight Co., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Camsight Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Camsight Co., Inc. in the registry?
The most recently registered devices listed for Camsight Co., Inc. include CDMX-H, OPTI, OPTUM, INTRAORAL CAMERA SYSTEM and CDMX.