Remedy Logic, Inc.
Country not established
- Devices
- 1
What Remedy Logic, Inc. makes
Remedy Logic, Inc. develops an AI-powered software tool, the RemedyLogic AI MRI Lumbar Spine Reader, designed to analyze and interpret MRI images of the lumbar spine for diagnostic purposes.
The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) clearance pathway. The product is based in the United States.
Catalogue
RemedyLogic AI MRI Lumbar Spine Reader Ref K241108
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Remedy Logic, Inc. have in the registry?
The registry currently lists 1 device for Remedy Logic, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Remedy Logic, Inc.'s devices?
Among its 1 most recently registered device, Remedy Logic, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Remedy Logic, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Remedy Logic, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Remedy Logic, Inc. in the registry?
The most recently registered devices listed for Remedy Logic, Inc. include RemedyLogic AI MRI Lumbar Spine Reader.