Dann Overseas, Inc.
Country not established
- Devices
- 1
What Dann Overseas, Inc. makes
Dann Overseas, Inc. manufactures latex patient examination gloves, designed for use in clinical settings to maintain hygiene and reduce infection risk during medical procedures.
These products are classified as Class I medical 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 K892790
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dann Overseas, Inc. have in the registry?
The registry currently lists 1 device for Dann Overseas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dann Overseas, Inc.'s devices?
Among its 1 most recently registered device, Dann Overseas, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dann Overseas, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dann Overseas, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dann Overseas, Inc. in the registry?
The most recently registered devices listed for Dann Overseas, Inc. include PATIENT EXAMINATION GLOVES (LATEX).