Toyobo Co., Ltd.
JapanFDA applicant, unverified
- Devices
- 7
What Toyobo Co., Ltd. makes
Toyobo Co., Ltd. manufactures the NERBRIDGE, a medical device designed for neural signal bridging applications, likely used in neurostimulation or neuromodulation therapies.
The NERBRIDGE is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
Nerbridge Ref K152967
Regimes: 510(k) Registry: 510(k)GUDID
Company details
- DUNS number
- 690538160
- [email protected]
- Phone
- +818025456900
Frequently asked questions
How many devices does Toyobo Co., Ltd. have in the registry?
The registry currently lists 7 devices for Toyobo Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Toyobo Co., Ltd.'s devices?
Among its 7 most recently registered devices, Toyobo Co., Ltd. has devices listed in FDA 510(k) (1 device) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Toyobo Co., Ltd.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Toyobo Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Toyobo Co., Ltd. in the registry?
The most recently registered devices listed for Toyobo Co., Ltd. include Nerbridge® RN00525E, Nerbridge® RN01025E, Nerbridge® RN04025E and Nerbridge® RN01525E.