Enterra Medical, Inc.
United Statesfrom the FDA registration address FDA FEI 3027386225
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
Company details
- FDA FEI number
- 3027386225
- DUNS number
- 118781894
- Address
- 5353 Wayzata Blvd., Saint Louis Park, MN, 55416
- Website
- www.enterramedical.com
- Phone
- 855-768-3772
From the company website
Enterra® Therapy is a surgical option for people unable to control chronic symptoms of gastroparesis. Enterra Medical is a dedicated team with a singular focus: to help more people suffering from chronic gastroparesis live better lives through advancing technology and accelerating access to the Enterra Therapy.
Frequently asked questions
How many devices does Enterra Medical, Inc. have in the registry?
The registry currently lists 1 device for Enterra Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Enterra Medical, Inc.'s devices?
Among its 1 most recently registered device, Enterra Medical, Inc. has devices listed in FDA GUDID (1 device).
What are the newest devices from Enterra Medical, Inc. in the registry?
The most recently registered devices listed for Enterra Medical, Inc. include Enterra ReliaStim Unipolar Lead 30101.