1World Vista Medical
FDA registration: United States Last updated 23 May 2026
- Devices
- 1
- Registries
- FDA 510(k)
- FDA recalls
- 0
Catalogue
What 1World Vista Medical makes
1World Vista Medical produces the SteriHub™ Disinfecting Device and Protective Cover, a system designed for disinfecting and protecting medical equipment to reduce contamination risks.
The SteriHub™ falls under FDA Class II regulation and is listed via the 510(k) pathway. The company is based in the United States.
Frequently asked questions
What types of medical devices does 1World Vista Medical manufacture?
1World Vista Medical specializes in the SteriHub™ Disinfecting Device and Protective Cover, a system intended to disinfect and protect medical equipment. This product is designed to help reduce contamination risks in healthcare settings.
Where is 1World Vista Medical based?
1World Vista Medical is based in the United States. The company’s location is relevant for understanding its regulatory framework and operational reach.
How are the devices manufactured by 1World Vista Medical classified by regulatory authorities?
The SteriHub™ Disinfecting Device and Protective Cover falls under FDA Class II classification. This classification is used for devices that pose moderate risk and require special controls to ensure safety and effectiveness.
Which regulatory registries or databases list the devices produced by 1World Vista Medical?
The SteriHub™ Disinfecting Device and Protective Cover is listed via the FDA’s 510(k) pathway, which is a premarket submission required for most Class II devices to demonstrate substantial equivalence to a legally marketed predicate device.
Information
- FDA registration
- United States