Fadr Intl., Inc.
Country not established
- Devices
- 1
What Fadr Intl., Inc. makes
Fadr Intl., Inc. manufactures latex patient examination gloves designed for clinical use, providing a barrier between healthcare providers and patients during medical examinations.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K892621
510(k) 510(k)
Frequently asked questions
How many devices does Fadr Intl., Inc. have in the registry?
The registry currently lists 1 device for Fadr Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fadr Intl., Inc.'s devices?
Among its 1 most recently registered device, Fadr Intl., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fadr Intl., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fadr Intl., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Fadr Intl., Inc. in the registry?
The most recently registered devices listed for Fadr Intl., Inc. include PATIENT EXAMINATION GLOVES (LATEX).