Lily Corp.
Country not established
- Devices
- 1
What Lily Corp. makes
Lily Corp. manufactures latex patient examination gloves, designed for clinical use to maintain hygiene and reduce infection risk during medical procedures.
These gloves are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891447
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Lily Corp. have in the registry?
The registry currently lists 1 device for Lily Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Lily Corp.'s devices?
Among its 1 most recently registered device, Lily Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Lily Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Lily Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Lily Corp. in the registry?
The most recently registered devices listed for Lily Corp. include PATIENT EXAMINATION GLOVES (LATEX).