Bluff City Medical Technologies, Inc.
Country not established
- Devices
- 1
What Bluff City Medical Technologies, Inc. makes
Bluff City Medical Technologies, Inc. manufactures tympanostomy tubes, which are small medical devices inserted into the eardrum to relieve pressure and improve hearing in cases of chronic ear infections or fluid buildup.
The company’s tympanostomy tubes are classified as Class II devices under FDA regulations and are listed via the 510(k) premarket notification process. The devices are based in the United States.
Catalogue
Tympanostomy Tube Ref K953802
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bluff City Medical Technologies, Inc. have in the registry?
The registry currently lists 1 device for Bluff City Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bluff City Medical Technologies, Inc.'s devices?
Among its 1 most recently registered device, Bluff City Medical Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bluff City Medical Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bluff City Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bluff City Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Bluff City Medical Technologies, Inc. include TYMPANOSTOMY TUBE.