Gregory S. Jacob, D.D.S.
Country not established
- Devices
- 1
What Gregory S. Jacob, D.D.S. makes
The company manufactures portable light curing units, which are handheld devices used in dental procedures to harden tooth restorative materials using ultraviolet or visible light.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer operates from the United States.
Catalogue
Portable Light Curing Unit Ref K994048
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gregory S. Jacob, D.D.S. have in the registry?
The registry currently lists 1 device for Gregory S. Jacob, D.D.S.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gregory S. Jacob, D.D.S.'s devices?
Among its 1 most recently registered device, Gregory S. Jacob, D.D.S. has devices listed in FDA 510(k) (1 device).
What risk classes do Gregory S. Jacob, D.D.S.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gregory S. Jacob, D.D.S.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gregory S. Jacob, D.D.S. in the registry?
The most recently registered devices listed for Gregory S. Jacob, D.D.S. include PORTABLE LIGHT CURING UNIT.