Ben Venue Laboratories, Inc.
Country not established
- Devices
- 1
What Ben Venue Laboratories, Inc. makes
Ben Venue Laboratories, Inc. manufactures ethylene oxide gas sterilization systems designed for medical device decontamination, including the ETHYLENE OXIDE GAS STERILIZATION SYS II. These systems are engineered for automated, high-volume sterilization of heat-sensitive items using ethylene oxide gas under controlled conditions.
The company’s portfolio is regulated under the FDA’s Class II device classification, with individual products authorised through the 510(k) clearance pathway. These systems are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations. The manufacturer operates from the United States.
Catalogue
Ethylene Oxide Gas Steriliza Sys Ii Ref K833457
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ben Venue Laboratories, Inc. have in the registry?
The registry currently lists 1 device for Ben Venue Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ben Venue Laboratories, Inc.'s devices?
Among its 1 most recently registered device, Ben Venue Laboratories, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ben Venue Laboratories, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ben Venue Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ben Venue Laboratories, Inc. in the registry?
The most recently registered devices listed for Ben Venue Laboratories, Inc. include ETHYLENE OXIDE GAS STERILIZA SYS II.