The Orient Connection
Country not established
- Devices
- 1
What The Orient Connection makes
The Orient Connection manufactures latex patient examination gloves, designed for clinical use to maintain hygiene and reduce infection risk during medical procedures.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892080
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Orient Connection have in the registry?
The registry currently lists 1 device for The Orient Connection. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Orient Connection's devices?
Among its 1 most recently registered device, The Orient Connection has devices listed in FDA 510(k) (1 device).
What risk classes do The Orient Connection's devices fall under?
Among its 1 most recently registered device, the classes recorded for The Orient Connection's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from The Orient Connection in the registry?
The most recently registered devices listed for The Orient Connection include PATIENT EXAMINATION GLOVES (LATEX).