Medtimo, Inc.
United Statesfrom the FDA registration address FDA FEI 3013508647
- Devices
- 38
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What Medtimo, Inc. makes
Medtimo, Inc. manufactures the Obalon Touch Inflation System, a device used for weight management via gastric inflation, and the LAP-BAND Adjustable Gastric Banding System, a restrictive bariatric implant designed to limit stomach capacity.
These devices are classified as Class III under FDA regulations and are listed under the Premarket Approval (PMA) pathway. The company is based in the United States.
Catalogue
Search and filter all 38 devicesCompany details
- FDA FEI number
- 3013508647
- DUNS number
- 144843751
- Address
- 7625 Golden Triangle Dr Ste G, Eden Prairie, MN, 55344
- [email protected]
- Phone
- 1-844-362-2566
Frequently asked questions
How many devices does Medtimo, Inc. have in the registry?
The registry currently lists 38 devices for Medtimo, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medtimo, Inc.'s devices?
Among its 38 most recently registered devices, Medtimo, Inc. has devices listed in FDA PMA (2 devices) and FDA GUDID (36 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Medtimo, Inc.'s devices fall under?
Among its 38 most recently registered devices, the classes recorded for Medtimo, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Medtimo, Inc. in the registry?
The most recently registered devices listed for Medtimo, Inc. include ReShape Calibration Tubes™ B-2017, OBALON® 7402-0001, Gastric Balloon Suction Catheter B-2020 and OBALON® Placebo Capsule 7150-0003.