Omni Sales Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Omni Sales Corp. makes
Omni Sales Corp. manufactures powder-free latex examination gloves designed for medical and clinical use, intended to provide a secure grip during procedures while minimizing powder-related risks.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Omni Grip Latex Examination Glove, Powder-Free Ref K964563
Regimes: 510(k) Registry: 510(k)Omni Grip Latex Examination Glove, Powder-Free Ref K970297
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omni Sales Corp. have in the registry?
The registry currently lists 2 devices for Omni Sales Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omni Sales Corp.'s devices?
Among its 2 most recently registered devices, Omni Sales Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Omni Sales Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Omni Sales Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Omni Sales Corp. in the registry?
The most recently registered devices listed for Omni Sales Corp. include OMNI GRIP LATEX EXAMINATION GLOVE, POWDER-FREE.