Preceptis Medical
Country not established
- Devices
- 12
What Preceptis Medical makes
Preceptis Medical designs and manufactures tympanostomy tube systems and associated insertion tools, including the Hummingbird Tympanostomy Tube System and the Preceptis Tympanostomy Tube Insertion Device. These products are intended for use in the placement of ventilation tubes in the middle ear to treat conditions such as chronic otitis media with effusion.
The company’s portfolio is regulated under FDA Class II devices and is listed in the FDA’s 510(k) and Unique Device Identifier (UDI) registries. The products are based in the United States.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Preceptis Medical have in the registry?
The registry currently lists 12 devices for Preceptis Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Preceptis Medical's devices?
Among its 12 most recently registered devices, Preceptis Medical has devices listed in FDA 510(k) (5 devices) and FDA GUDID (7 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Preceptis Medical's devices fall under?
Among its 12 most recently registered devices, the classes recorded for Preceptis Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Preceptis Medical in the registry?
The most recently registered devices listed for Preceptis Medical include Hummingbird Tympanostomy Tube System 05-1001-752, Hummingbird Tympanostomy Tube System 05-1001-753, Hummingbird Tympanostomy Tube System 05-1001-501 and Hummingbird Tympanostomy Tube System 05-1001-503.