Audra, Inc.
Country not established
- Devices
- 1
What Audra, Inc. makes
Audra, Inc. manufactures latex patient examination gloves designed for clinical use, providing a barrier between healthcare providers and patients during medical examinations.
The company’s latex examination gloves are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The products are intended for use in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891353
510(k) 510(k)
Frequently asked questions
How many devices does Audra, Inc. have in the registry?
The registry currently lists 1 device for Audra, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Audra, Inc.'s devices?
Among its 1 most recently registered device, Audra, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Audra, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Audra, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Audra, Inc. in the registry?
The most recently registered devices listed for Audra, Inc. include PATIENT EXAMINATION GLOVES (LATEX).