Adri
Country not established
- Devices
- 6
What Adri makes
Adri manufactures topical wound dressings, including alginate fiber and foam-based products with or without collagen, as well as silver-impregnated alginate dressings for exuding wounds. These products are designed to absorb wound exudate and promote a moist healing environment.
The company’s portfolio is regulated under FDA Class I and Class II (U) devices, with several products cleared via the 510(k) pathway. These dressings are listed in the FDA’s 510(k) database and are intended for use in the United States.
Catalogue
Alginate Fiber Topical Wound Dressing Ref K940404
Regimes: 510(k) Registry: 510(k)Foam Calcium Aliginate Topical Wound Dressing Ref K963656
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Silversite Or Calgitrol Ref K041268
Regimes: 510(k) Registry: 510(k)Alginate Wool Fiber Ref K870383
Regimes: 510(k) Registry: 510(k)Calgitrol AG Silver Alginate Wound Dressing Ref K011618
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adri have in the registry?
The registry currently lists 6 devices for Adri. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adri's devices?
Among its 6 most recently registered devices, Adri has devices listed in FDA 510(k) (6 devices).
What risk classes do Adri's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Adri's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Adri in the registry?
The most recently registered devices listed for Adri include ALGINATE FIBER TOPICAL WOUND DRESSING, FOAM CALCIUM ALIGINATE TOPICAL WOUND DRESSING, FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN and SILVERSITE OR CALGITROL.