Entreprise Premont, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Entreprise Premont, Inc. makes
Entreprise Premont, Inc. manufactures the Humask Pro Vision and Humask Pro Vision 3000, which are medical-grade face masks.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Humask Pro Vision, Humask Pro Vision 3000 Ref K222551
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Entreprise Premont, Inc. have in the registry?
The registry currently lists 1 device for Entreprise Premont, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Entreprise Premont, Inc.'s devices?
Among its 1 most recently registered device, Entreprise Premont, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Entreprise Premont, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Entreprise Premont, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Entreprise Premont, Inc. in the registry?
The most recently registered devices listed for Entreprise Premont, Inc. include Humask Pro Vision, Humask Pro Vision 3000.