Xylos Corporation
United StatesFDA 510(k) applicant, unverified
- Devices
- 9
What Xylos Corporation makes
Xylos Corporation manufactures wound care dressings, including antimicrobial and porous varieties, as well as surgical meshes designed for tissue reinforcement and vascular applications. Their portfolio includes protective sheets for medical treatments, vessel guards for surgical procedures, and modified mesh variants for specific clinical needs.
The company’s devices are regulated under FDA Class II and Class U classifications, with most products authorised via the 510(k) pathway. These products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
X-Cell Wound Dressing Ref K974251
510(k) 510(k)Xylos Vessel Guard Ref K100984
510(k) 510(k)Xylos Surgical Mesh Ref K023237
510(k) 510(k)Xylos Porous Surgical Mesh Ref K090880
510(k) 510(k)Modification To Xylos Surgical Mesh Ref K081882
510(k) 510(k)Xylos Macro-Porous Surgical Mesh Ref K111584
510(k) 510(k)Mta Protective Sheet Ref K090778
510(k) 510(k)Securian Tissue Reinforcement Matrix Ref K083823
510(k) 510(k)Xylos Xcell Antimicrobial Dressing Ref K024054
510(k) 510(k)
Frequently asked questions
How many devices does Xylos Corporation have in the registry?
The registry currently lists 9 devices for Xylos Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xylos Corporation's devices?
Among its 9 most recently registered devices, Xylos Corporation has devices listed in FDA 510(k) (9 devices).
What risk classes do Xylos Corporation's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Xylos Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Xylos Corporation in the registry?
The most recently registered devices listed for Xylos Corporation include X-CELL WOUND DRESSING, XYLOS VESSEL GUARD, XYLOS SURGICAL MESH and XYLOS POROUS SURGICAL MESH.