Sangi Co., Ltd.
JapanFDA applicant, unverified
- Devices
- 2
What Sangi Co., Ltd. makes
Sangi Co., Ltd. manufactures dental products designed to reduce tooth sensitivity, including a remineralizing toothpaste for home use and a professional-grade desensitizer.
These products are regulated as Class II medical devices in the U.S. and are listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Apapro Desensitizer Ref K220419
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sangi Co., Ltd. have in the registry?
The registry currently lists 2 devices for Sangi Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sangi Co., Ltd.'s devices?
Among its 2 most recently registered devices, Sangi Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Sangi Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sangi Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sangi Co., Ltd. in the registry?
The most recently registered devices listed for Sangi Co., Ltd. include APAPRO Desensitizer Homecare (Remineralizing Anti-sensitivity Toothpaste) and Apapro Desensitizer.