Honeynaps Co., Ltd.
South KoreaFDA applicant, unverified
- Devices
- 2
What Honeynaps Co., Ltd. makes
Honeynaps Co., Ltd. manufactures the SOMNUM (Version 1.1.2.), a medical device designed for sleep monitoring and analysis, likely incorporating sensors and software to track physiological parameters during sleep.
The SOMNUM device is classified as Class II under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Somnum (Somnum) Ref K253390
Regimes: 510(k) Registry: 510(k)Somnum (V.1.1.2.) Ref K223922
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Honeynaps Co., Ltd. have in the registry?
The registry currently lists 2 devices for Honeynaps Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Honeynaps Co., Ltd.'s devices?
Among its 2 most recently registered devices, Honeynaps Co., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Honeynaps Co., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Honeynaps Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Honeynaps Co., Ltd. in the registry?
The most recently registered devices listed for Honeynaps Co., Ltd. include SOMNUM (SOMNUM) and SOMNUM (V.1.1.2.).