Dunmore Corp.
Country not established
- Devices
- 1
What Dunmore Corp. makes
Dunmore Corp. manufactures medical devices specifically designed for the treatment of hemorrhoids, targeting symptomatic relief and procedural interventions in this condition.
These devices are classified under Class II (U) in the U.S. regulatory framework and are listed via the FDA’s 510(k) pathway. The company’s portfolio is regulated under U.S. jurisdiction, with no additional international listings referenced.
Catalogue
Device For The Treatment Of Hemorrhoids Ref K822649
510(k) 510(k)
Frequently asked questions
How many devices does Dunmore Corp. have in the registry?
The registry currently lists 1 device for Dunmore Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dunmore Corp.'s devices?
Among its 1 most recently registered device, Dunmore Corp. has devices listed in FDA 510(k) (1 device).
What are the newest devices from Dunmore Corp. in the registry?
The most recently registered devices listed for Dunmore Corp. include DEVICE FOR THE TREATMENT OF HEMORRHOIDS.