Reddress Ltd
Country not established FDA
Part of RedDress LTD
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA establishment
What Reddress Ltd makes
Reddress Ltd manufactures a wound therapy device designed for the preparation of autologous blood clots, intended for use in wound care applications. The product, ActiGraft, is a kit that processes a patient’s own blood to create clots for localized treatment.
The company’s portfolio is regulated under Class II medical devices in the United States, with devices listed in the FDA’s Unique Device Identifier (UDI) database. Reddress Ltd operates from the US, adhering to applicable regulatory requirements for Class II wound therapy products.
Catalogue
- GUDID
Company details
- DUNS number
- 533179532
FDA establishments
- RedDress LTD Pardes Hanna Haifa · IL FEI 3015399811
Frequently asked questions
How many devices does REDDRESS LTD have in the registry?
The registry currently lists 1 device for REDDRESS LTD. Devices recorded under merged duplicate company entries are counted once.
Which registries list REDDRESS LTD's devices?
Among its 1 most recently registered device, REDDRESS LTD has devices listed in FDA GUDID (1 device).
What risk classes do REDDRESS LTD's devices fall under?
Among its 1 most recently registered device, the classes recorded for REDDRESS LTD's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from REDDRESS LTD in the registry?
The most recently registered devices listed for REDDRESS LTD include ActiGraft RD2201.
Which FDA establishments are linked to REDDRESS LTD?
1 FDA establishment is linked to REDDRESS LTD in the registry; they are listed on the company page.