Omni Intl., Inc.
United StatesFDA applicant, unverified
- Devices
- 12
What Omni Intl., Inc. makes
Omni Intl., Inc. manufactures surgical and medical accessories, including clamps for medical tubing, implantable devices, nerve stimulators, and protective transducers. Their portfolio also covers nasal oxygen cannulas, intravenous administration sets, surgical gowns, and latex surgical gloves with powder-free formulations. Transcutaneous electrical nerve stimulators (TENS) and stimulator devices are part of their product line.
The company’s devices are regulated under FDA Class I and Class II classifications, with several listed via the 510(k) pathway. Products are distributed in the United States, where Omni Intl., Inc. is based.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Omni Intl., Inc. have in the registry?
The registry currently lists 12 devices for Omni Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omni Intl., Inc.'s devices?
Among its 12 most recently registered devices, Omni Intl., Inc. has devices listed in FDA 510(k) (12 devices).
What risk classes do Omni Intl., Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Omni Intl., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omni Intl., Inc. in the registry?
The most recently registered devices listed for Omni Intl., Inc. include OMNIMED CLAMP, F-SERIES IMPLANT, OMNIPROBE ELECTRICAL NERVE STIMULATOR and OMNIMED SUPERIOR TRANSDUCER PROTECTOR.