Arnold & Sons
Country not established
- Devices
- 1
What Arnold & Sons makes
Arnold & Sons manufactures portable autoclaves designed for sterilization of medical instruments and supplies in clinical or field settings. These devices use steam under pressure to eliminate pathogens, supporting infection control in environments where traditional autoclaves are impractical.
The company’s portable autoclaves are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The products are intended for use in the United States, where compliance with FDA requirements is mandatory. No additional registries or international listings are referenced.
Catalogue
Portable Autoclaves Ref K830931
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arnold & Sons have in the registry?
The registry currently lists 1 device for Arnold & Sons. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arnold & Sons's devices?
Among its 1 most recently registered device, Arnold & Sons has devices listed in FDA 510(k) (1 device).
What risk classes do Arnold & Sons's devices fall under?
Among its 1 most recently registered device, the classes recorded for Arnold & Sons's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arnold & Sons in the registry?
The most recently registered devices listed for Arnold & Sons include PORTABLE AUTOCLAVES.