Laminar Digital Health, Inc.
Country not established
- Devices
- 1
What Laminar Digital Health, Inc. makes
Laminar Digital Health, Inc. manufactures the Laminar P1 (LDH-HW-001), a medical device designed for digital health monitoring and remote patient assessment, enabling real-time data collection and analysis.
The Laminar P1 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Laminar P1 (LDH-HW-001) Ref K242487
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Laminar Digital Health, Inc. have in the registry?
The registry currently lists 1 device for Laminar Digital Health, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Laminar Digital Health, Inc.'s devices?
Among its 1 most recently registered device, Laminar Digital Health, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Laminar Digital Health, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Laminar Digital Health, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Laminar Digital Health, Inc. in the registry?
The most recently registered devices listed for Laminar Digital Health, Inc. include Laminar P1 (LDH-HW-001).