Arnold Technologies
Country not established
- Devices
- 2
What Arnold Technologies makes
Arnold Technologies manufactures a combination night drainage unit, designed for continuous urinary drainage during sleep, and a personal punch device, intended for manual tissue or wound management.
The company’s products are classified as Class I medical devices under FDA regulations, with records supported by 510(k) submissions. These devices are listed in the U.S. regulatory system.
Catalogue
Combination Nite Drainage Unit Ref K872294
Regimes: 510(k) Registry: 510(k)Personal Punch Ref K870136
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arnold Technologies have in the registry?
The registry currently lists 2 devices for Arnold Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arnold Technologies's devices?
Among its 2 most recently registered devices, Arnold Technologies has devices listed in FDA 510(k) (2 devices).
What risk classes do Arnold Technologies's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Arnold Technologies's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Arnold Technologies in the registry?
The most recently registered devices listed for Arnold Technologies include COMBINATION NITE DRAINAGE UNIT and PERSONAL PUNCH.