EzaLife Inc.
Country not established FDA establishment FEI 3039644422
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
What EzaLife Inc. makes
EzaLife Inc. manufactures wearable percutaneous catheter/tube holders designed to secure medical lines to a patient’s clothing, reducing the risk of dislodgement or infection. The Button Huggie is a key product in this category, providing a discreet, adhesive-free attachment method for catheters or tubes.
The company’s wearable percutaneous catheter/tube holder is classified as Class II under FDA regulations and is listed in the FDA Unique Device Identifier (UDI) database. The product is intended for use in the United States.
Catalogue
- GUDID
- GUDID
Company details
- FDA FEI number
- 3039644422
- Address
- 12635 E Montview Blvd Ste 100, Aurora, CO, 80045
Frequently asked questions
How many devices does EzaLife Inc. have in the registry?
The registry currently lists 2 devices for EzaLife Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list EzaLife Inc.'s devices?
Among its 2 most recently registered devices, EzaLife Inc. has devices listed in FDA GUDID (2 devices).
What risk classes do EzaLife Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for EzaLife Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from EzaLife Inc. in the registry?
The most recently registered devices listed for EzaLife Inc. include Button Huggie Version 1 for AMT MiniONE G-Button.