Xytex Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Xytex Corp. makes
Xytex Corp. manufactures corneal preservation and dehydration systems, including units designed to store and process corneal tissue using glycerine-based dehydration for transplantation purposes.
The company’s portfolio is classified under FDA Class II devices and is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Cornea Perservation Unit Ref K821170
510(k) 510(k)Glycerine Dehydration Unit Ref K810400
510(k) 510(k)
Frequently asked questions
How many devices does Xytex Corp. have in the registry?
The registry currently lists 2 devices for Xytex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Xytex Corp.'s devices?
Among its 2 most recently registered devices, Xytex Corp. has devices listed in FDA 510(k) (2 devices).
What are the newest devices from Xytex Corp. in the registry?
The most recently registered devices listed for Xytex Corp. include CORNEA PERSERVATION UNIT and GLYCERINE DEHYDRATION UNIT.