Indigo Orb, Inc.
Country not established
- Devices
- 1
What Indigo Orb, Inc. makes
Indigo Orb, Inc. manufactures the Autodetect Syringe, a device designed for automated detection and monitoring of syringe usage, likely in clinical or medical settings.
The Autodetect Syringe is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Autodetect Syringe Ref K041590
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Indigo Orb, Inc. have in the registry?
The registry currently lists 1 device for Indigo Orb, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Indigo Orb, Inc.'s devices?
Among its 1 most recently registered device, Indigo Orb, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Indigo Orb, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Indigo Orb, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Indigo Orb, Inc. in the registry?
The most recently registered devices listed for Indigo Orb, Inc. include AUTODETECT SYRINGE.