Omniguide Communications, Inc.
Country not established
- Devices
- 1
What Omniguide Communications, Inc. makes
Omniguide Communications, Inc. manufactures the OMNIGUIDE BEAMPATH CO2 MARK I, a device designed for laser beam delivery in medical procedures.
The company’s portfolio is regulated under Class II medical devices in the US and includes products listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omniguide Communications, Inc. have in the registry?
The registry currently lists 1 device for Omniguide Communications, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omniguide Communications, Inc.'s devices?
Among its 1 most recently registered device, Omniguide Communications, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Omniguide Communications, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omniguide Communications, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omniguide Communications, Inc. in the registry?
The most recently registered devices listed for Omniguide Communications, Inc. include OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY.