Mint Labs, Inc., D/B/A. Qmenta
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- Devices
- 1
What Mint Labs, Inc., D/B/A. Qmenta makes
Mint Labs, Inc. (d/b/a Qmenta) develops the Qmenta Care Platform Family, a digital health solution designed for remote patient monitoring and clinical decision support in respiratory care.
The company’s portfolio is regulated under FDA’s Class II device classification, with devices authorised via the 510(k) pathway. The platform is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Qmenta Care Platform Family Ref K202718
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mint Labs, Inc., D/B/A. Qmenta have in the registry?
The registry currently lists 1 device for Mint Labs, Inc., D/B/A. Qmenta. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mint Labs, Inc., D/B/A. Qmenta's devices?
Among its 1 most recently registered device, Mint Labs, Inc., D/B/A. Qmenta has devices listed in FDA 510(k) (1 device).
What risk classes do Mint Labs, Inc., D/B/A. Qmenta's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mint Labs, Inc., D/B/A. Qmenta's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mint Labs, Inc., D/B/A. Qmenta in the registry?
The most recently registered devices listed for Mint Labs, Inc., D/B/A. Qmenta include Qmenta Care Platform Family.