Mobile Dental Equipment Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Mobile Dental Equipment Corp. makes
Mobile Dental Equipment Corp. manufactures portable dental X-ray systems, including the PORT OPII, PORT OPIII, PORT-XD, and PORT-XP. These devices are designed for intraoral and extraoral imaging, supporting dental diagnostics in mobile or clinic settings.
The company’s products are regulated under FDA Class I and Class II designations, with submissions recorded in the FDA 510(k) registry. The portfolio is listed in the US market under these regulatory pathways.
Catalogue
Port Opii, Port Opiii Ref K923354
Regimes: 510(k) Registry: 510(k)Port-Xd Ref K923360
Regimes: 510(k) Registry: 510(k)Port-Xp Ref K923359
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mobile Dental Equipment Corp. have in the registry?
The registry currently lists 3 devices for Mobile Dental Equipment Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mobile Dental Equipment Corp.'s devices?
Among its 3 most recently registered devices, Mobile Dental Equipment Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Mobile Dental Equipment Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Mobile Dental Equipment Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mobile Dental Equipment Corp. in the registry?
The most recently registered devices listed for Mobile Dental Equipment Corp. include PORT OPII, PORT OPIII, PORT-XD and PORT-XP.