Professional Technologies Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Professional Technologies Corp. makes
Professional Technologies Corp. manufactures the MMAC II Tonometer, a device used for measuring intraocular pressure in the eye, and Dentin Relief, a product designed to provide temporary relief from tooth sensitivity.
The company’s portfolio is regulated under FDA’s Class II device classification, with devices listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Mmac Ii Tonometer Ref K884012
Regimes: 510(k) Registry: 510(k)Dentin Relief Ref K924670
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Professional Technologies Corp. have in the registry?
The registry currently lists 2 devices for Professional Technologies Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Professional Technologies Corp.'s devices?
Among its 2 most recently registered devices, Professional Technologies Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Professional Technologies Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Professional Technologies Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Professional Technologies Corp. in the registry?
The most recently registered devices listed for Professional Technologies Corp. include MMAC II TONOMETER and DENTIN RELIEF.