Axon Instruments, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 3
What Axon Instruments, Inc. makes
Axon Instruments, Inc. manufactures the MM-1 Movement Monitor, a device for tracking and recording motion parameters, and the Guideline System, a tool for precise anatomical or experimental guidance. The company also produces the Axon MP-1 Micropositioner, designed for fine adjustments in laboratory or research settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Mm-1 Movement Monitor Ref K971318
510(k) 510(k)Guideline System Ref K970943
510(k) 510(k)Axon Mp-1 Micropositioner Ref K990683
510(k) 510(k)
Frequently asked questions
How many devices does Axon Instruments, Inc. have in the registry?
The registry currently lists 3 devices for Axon Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Axon Instruments, Inc.'s devices?
Among its 3 most recently registered devices, Axon Instruments, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Axon Instruments, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Axon Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Axon Instruments, Inc. in the registry?
The most recently registered devices listed for Axon Instruments, Inc. include MM-1 MOVEMENT MONITOR, GUIDELINE SYSTEM and AXON MP-1 MICROPOSITIONER.