Orioxi Intl. Corp.
Country not established
- Devices
- 1
What Orioxi Intl. Corp. makes
Orioxi Intl. Corp. manufactures latex patient examination gloves designed for clinical use, providing a barrier between healthcare providers and patients during medical examinations.
The company’s product portfolio is classified under FDA’s Class I regulatory category and is listed via the 510(k) clearance process in the United States. The company is based in the US.
Catalogue
Patient Examination Gloves (Latex) Ref K891442
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Orioxi Intl. Corp. have in the registry?
The registry currently lists 1 device for Orioxi Intl. Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Orioxi Intl. Corp.'s devices?
Among its 1 most recently registered device, Orioxi Intl. Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Orioxi Intl. Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Orioxi Intl. Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Orioxi Intl. Corp. in the registry?
The most recently registered devices listed for Orioxi Intl. Corp. include PATIENT EXAMINATION GLOVES (LATEX).