Cypress Ent.
Country not established
- Devices
- 1
What Cypress Ent. makes
Cypress Ent. manufactures patient examination gloves, designed for single-use medical procedures to maintain hygiene and reduce infection risk during clinical examinations.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves Ref K892992
510(k) 510(k)
Frequently asked questions
How many devices does Cypress Ent. have in the registry?
The registry currently lists 1 device for Cypress Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cypress Ent.'s devices?
Among its 1 most recently registered device, Cypress Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do Cypress Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cypress Ent.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cypress Ent. in the registry?
The most recently registered devices listed for Cypress Ent. include PATIENT EXAMINATION GLOVES.