Alcove Medical, Inc.
United Statesfrom the FDA registration address FDA FEI 3046548163
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Alcove Medical, Inc. makes
Alcove Medical, Inc. manufactures the NEO 2 LINE SUCTION SYSTEM, a device designed for medical suctioning applications in clinical settings.
The NEO 2 LINE SUCTION SYSTEM is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Neo 2 Line Suction System Ref K960488
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3046548163
- Address
- 2318 N Wonser, Cedar City, UT, 84721
Frequently asked questions
How many devices does Alcove Medical, Inc. have in the registry?
The registry currently lists 1 device for Alcove Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Alcove Medical, Inc.'s devices?
Among its 1 most recently registered device, Alcove Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Alcove Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Alcove Medical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Alcove Medical, Inc. in the registry?
The most recently registered devices listed for Alcove Medical, Inc. include NEO 2 LINE SUCTION SYSTEM.