Orbitec Technologies Corp.
Country not established
- Devices
- 1
What Orbitec Technologies Corp. makes
Orbitec Technologies Corp. manufactures the PED ALERT, which is a medical device.
The company is based in the US, and its portfolio includes Class II devices that are listed in the FDA 510(k) registry.
Catalogue
Ped Alert Ref K950656
510(k) 510(k)
Frequently asked questions
How many devices does Orbitec Technologies Corp. have in the registry?
The registry currently lists 1 device for Orbitec Technologies Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orbitec Technologies Corp.'s devices?
Among its 1 most recently registered device, Orbitec Technologies Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Orbitec Technologies Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orbitec Technologies Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Orbitec Technologies Corp. in the registry?
The most recently registered devices listed for Orbitec Technologies Corp. include PED ALERT.