Greg and Greg, Inc.
Country not established
- Devices
- 1
What Greg and Greg, Inc. makes
Greg and Greg, Inc. manufactures Class I medical devices, including multiple products that fall under this category.
The company's devices are listed in the FDA 510(k) registry and is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Multiple Ref K933616
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Greg and Greg, Inc. have in the registry?
The registry currently lists 1 device for Greg and Greg, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Greg and Greg, Inc.'s devices?
Among its 1 most recently registered device, Greg and Greg, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Greg and Greg, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Greg and Greg, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Greg and Greg, Inc. in the registry?
The most recently registered devices listed for Greg and Greg, Inc. include MULTIPLE.