Ncl Corp.
Country not established
- Devices
- 1
What Ncl Corp. makes
Ncl Corp. manufactures ULTRA.SPEC non-sterile latex examination gloves, designed for single-use medical and clinical examinations. These gloves are intended to provide barrier protection during procedures requiring hand hygiene.
The company’s portfolio is regulated under FDA 510(k) clearance as Class I devices, meeting U.S. medical device compliance requirements. The products are listed in the FDA’s 510(k) database. Ncl Corp. is based in the United States.
Catalogue
Ultra.spec Non-Sterile Latex Examination Glove Ref K902282
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ncl Corp. have in the registry?
The registry currently lists 1 device for Ncl Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ncl Corp.'s devices?
Among its 1 most recently registered device, Ncl Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Ncl Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ncl Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ncl Corp. in the registry?
The most recently registered devices listed for Ncl Corp. include ULTRA.SPEC NON-STERILE LATEX EXAMINATION GLOVE.