Veratex Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Veratex Corp. makes
Veratex Corp. manufactures sterile surgical drapes, including 17×18-inch models with and without fenestrations, and sterile cotton rolls in size #3 (1½-inch diameter). These products are designed for use in surgical and procedural settings to maintain sterile fields and absorb fluids.
The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with products listed via the 510(k) pathway. Veratex Corp. is headquartered in the United States.
Catalogue
Sterile Drape 17X18 W/3 Fenestration Ref K801033
Regimes: 510(k) Registry: 510(k)Sterile Cotton Rolls #3, 1 1/2 Ref K830175
Regimes: 510(k) Registry: 510(k)Sterile Drape 17X18 Code D-6A Ref K801032
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Veratex Corp. have in the registry?
The registry currently lists 3 devices for Veratex Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Veratex Corp.'s devices?
Among its 3 most recently registered devices, Veratex Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Veratex Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Veratex Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Veratex Corp. in the registry?
The most recently registered devices listed for Veratex Corp. include STERILE DRAPE 17X18 W/3 FENESTRATION, STERILE COTTON ROLLS #3, 1 1/2 and STERILE DRAPE 17X18 CODE D-6A.