Thimble Bioelectronics, Inc.
Country not established
- Devices
- 1
What Thimble Bioelectronics, Inc. makes
Thimble Bioelectronics, Inc. manufactures the CUR Model 1, a bioelectronic device designed for non-invasive neuromodulation applications, targeting specific neural pathways to influence physiological responses.
The CUR Model 1 is classified as a Class II medical device under FDA regulations and has been authorised via the 510(k) pathway. The company is headquartered in the United States.
Catalogue
CUR Model 1 Ref K160052
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thimble Bioelectronics, Inc. have in the registry?
The registry currently lists 1 device for Thimble Bioelectronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thimble Bioelectronics, Inc.'s devices?
Among its 1 most recently registered device, Thimble Bioelectronics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Thimble Bioelectronics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Thimble Bioelectronics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thimble Bioelectronics, Inc. in the registry?
The most recently registered devices listed for Thimble Bioelectronics, Inc. include CUR Model 1.