Rockfield Medical
IrelandFDA applicant, unverified
- Devices
- 2
What Rockfield Medical makes
Rockfield Medical manufactures enteral feeding systems, including an over-the-counter (OTC) version and a prescription model designed for tube feeding support.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Mobility+ Enteral Feeding System OTC Ref K233034
Regimes: 510(k) Registry: 510(k)Mobility+ Enteral Feeding System Ref K222678
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rockfield Medical have in the registry?
The registry currently lists 2 devices for Rockfield Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rockfield Medical's devices?
Among its 2 most recently registered devices, Rockfield Medical has devices listed in FDA 510(k) (2 devices).
What risk classes do Rockfield Medical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Rockfield Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rockfield Medical in the registry?
The most recently registered devices listed for Rockfield Medical include Mobility+ Enteral Feeding System OTC and Mobility+ Enteral Feeding System.