Dr. Alan A. Lowe, Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Dr. Alan A. Lowe, Inc. makes
Dr. Alan A. Lowe, Inc. manufactures the Lowe Klearway, a medical device designed for use in orthopedic surgery to assist in the alignment and stabilization of bone fractures or joint replacements.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) premarket notifications. The manufacturer operates from the United States.
Catalogue
Lowe Klearway Ref K950763
510(k) 510(k)
Frequently asked questions
How many devices does Dr. Alan A. Lowe, Inc. have in the registry?
The registry currently lists 1 device for Dr. Alan A. Lowe, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dr. Alan A. Lowe, Inc.'s devices?
Among its 1 most recently registered device, Dr. Alan A. Lowe, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dr. Alan A. Lowe, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dr. Alan A. Lowe, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dr. Alan A. Lowe, Inc. in the registry?
The most recently registered devices listed for Dr. Alan A. Lowe, Inc. include LOWE KLEARWAY.