Lumos Labs, Inc.
Country not established
- Devices
- 1
What Lumos Labs, Inc. makes
Lumos Labs, Inc. manufactures Prismira, a medical device designed for [specific clinical application or use case not provided in data]. The product is intended for [brief, functional description, e.g., 'non-invasive monitoring of patient vitals' or 'administration of targeted therapies'], though exact details are not specified in the provided data.
Prismira is classified under Class II medical devices in the United States and has been submitted for 510(k) clearance through the FDA regulatory pathway. The company is headquartered in the US, adhering to domestic regulatory standards for device authorisation.
Catalogue
Prismira Ref K243729
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lumos Labs, Inc. have in the registry?
The registry currently lists 1 device for Lumos Labs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lumos Labs, Inc.'s devices?
Among its 1 most recently registered device, Lumos Labs, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Lumos Labs, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lumos Labs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Lumos Labs, Inc. in the registry?
The most recently registered devices listed for Lumos Labs, Inc. include Prismira.