Boehringer/Miter, Inc.
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- Devices
- 1
What Boehringer/Miter, Inc. makes
Boehringer/Miter, Inc. manufactures the TITANALOY SUBMERSIBLE IMPLANT SYSTEM, a device designed for subcutaneous or implantable use in medical procedures.
The company’s portfolio is regulated under FDA Class II devices, with the TITANALOY SUBMERSIBLE IMPLANT SYSTEM listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Titanaloy Submersible Implant System Ref K830414
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Boehringer/Miter, Inc. have in the registry?
The registry currently lists 1 device for Boehringer/Miter, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Boehringer/Miter, Inc.'s devices?
Among its 1 most recently registered device, Boehringer/Miter, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Boehringer/Miter, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Boehringer/Miter, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Boehringer/Miter, Inc. in the registry?
The most recently registered devices listed for Boehringer/Miter, Inc. include TITANALOY SUBMERSIBLE IMPLANT SYSTEM.