Omni Mfg., Inc.
Country not established
- Devices
- 1
What Omni Mfg., Inc. makes
Omni Mfg., Inc. manufactures the OMNISORB II, a sterile, nonwoven surgical sponge designed for use in medical procedures to absorb fluids and maintain hemostasis during surgery.
The OMNISORB II is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Omnisorb Ii, Nonwoven Sponge, Sterile And Non Ref K931610
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omni Mfg., Inc. have in the registry?
The registry currently lists 1 device for Omni Mfg., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omni Mfg., Inc.'s devices?
Among its 1 most recently registered device, Omni Mfg., Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Omni Mfg., Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Omni Mfg., Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Omni Mfg., Inc. in the registry?
The most recently registered devices listed for Omni Mfg., Inc. include OMNISORB II, NONWOVEN SPONGE, STERILE AND NON.