Je Liss & Co., Inc.
Country not established
- Devices
- 1
What Je Liss & Co., Inc. makes
Je Liss & Co., Inc. manufactures HEARIT, a medical device designed for hearing assessment or amplification, though specific clinical applications are not detailed.
The company’s portfolio is regulated under FDA’s Class II designation, with devices listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Hearit Ref K934805
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Je Liss & Co., Inc. have in the registry?
The registry currently lists 1 device for Je Liss & Co., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Je Liss & Co., Inc.'s devices?
Among its 1 most recently registered device, Je Liss & Co., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Je Liss & Co., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Je Liss & Co., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Je Liss & Co., Inc. in the registry?
The most recently registered devices listed for Je Liss & Co., Inc. include HEARIT.