Gravitas Medical, Inc.
United StatesFDA applicant, unverified FDA FEI 3034881464
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Gravitas Medical, Inc. makes
Gravitas Medical, Inc. manufactures enteral feeding tubes, including the Entarik NI Feeding Tube System and the Entarik Feeding Tube System, designed for nutritional support in patients requiring alternative feeding methods.
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
Entarik NI Feeding Tube System Ref K241169
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3034881464
- Address
- 2332 4th St Ste E, Berkeley, CA, 94710
Frequently asked questions
How many devices does Gravitas Medical, Inc. have in the registry?
The registry currently lists 2 devices for Gravitas Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gravitas Medical, Inc.'s devices?
Among its 2 most recently registered devices, Gravitas Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Gravitas Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Gravitas Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gravitas Medical, Inc. in the registry?
The most recently registered devices listed for Gravitas Medical, Inc. include Entarik NI Feeding Tube System and Entarik Feeding Tube System; Entarik Feeding Tube.