Kay Ent.
Country not established
- Devices
- 1
What Kay Ent. makes
Kay Ent. manufactures the Prenatal Wedge, a device designed to support pelvic alignment and reduce discomfort during pregnancy.
The Prenatal Wedge is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Prenatal Wedge Ref K895343
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kay Ent. have in the registry?
The registry currently lists 1 device for Kay Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kay Ent.'s devices?
Among its 1 most recently registered device, Kay Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do Kay Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Kay Ent.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kay Ent. in the registry?
The most recently registered devices listed for Kay Ent. include PRENATAL WEDGE.