Morwel Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Morwel Corp. makes
Morwel Corp. makes suction tips, an ultra-safe ultrasonic aspirator system, a Morwel aspirator, and a Morwel cannula.
These devices are classified as Class II, U and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Suction Tips Ref K841159
Regimes: 510(k) Registry: 510(k)Ultra-Safe Ultrasonic Aspirator System Ref K962525
Regimes: 510(k) Registry: 510(k)Morwel Aspirator Ref K841160
Regimes: 510(k) Registry: 510(k)Morwel Cannula Ref K831520
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Morwel Corp. have in the registry?
The registry currently lists 4 devices for Morwel Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Morwel Corp.'s devices?
Among its 4 most recently registered devices, Morwel Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Morwel Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Morwel Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Morwel Corp. in the registry?
The most recently registered devices listed for Morwel Corp. include SUCTION TIPS, ULTRA-SAFE ULTRASONIC ASPIRATOR SYSTEM, MORWEL ASPIRATOR and MORWEL CANNULA.