Misten Medical Corp.
United StatesFDA applicant, unverified
- Devices
- 4
What Misten Medical Corp. makes
Misten Medical Corp. manufactures surgical instruments and prostheses for otologic procedures, including vent tubes for middle ear drainage, a surgical drill for bone preparation, and partial/total ossicular replacement prostheses for hearing restoration.
The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Misten Medical Reuter Bobbin Style Vent Tube Ref K955616
Regimes: 510(k) Registry: 510(k)Misten Medical Misten Medical Surgical Drill Ref K962163
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Misten Medical Corp. have in the registry?
The registry currently lists 4 devices for Misten Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Misten Medical Corp.'s devices?
Among its 4 most recently registered devices, Misten Medical Corp. has devices listed in FDA 510(k) (4 devices).
What risk classes do Misten Medical Corp.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Misten Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Misten Medical Corp. in the registry?
The most recently registered devices listed for Misten Medical Corp. include MISTEN MEDICAL REUTER BOBBIN STYLE VENT TUBE, MISTEN MEDICAL MISTEN MEDICAL SURGICAL DRILL, MISTEN MEDICAL PARTIAL OSSICULAR REPLACEMENT PROSTHESIS and MISTEN MEDICAL TOTAL OSSICULAR REPLACEMENT PROSTHESIS.