Omni Surgical, L.P.
United StatesFDA applicant, unverified
- Devices
- 2
What Omni Surgical, L.P. makes
Omni Surgical, L.P. manufactures spinal fixation and interbody fusion devices, including anterior buttress plates and cervical, posterior lumbar interbody fusion (PLIF), transforaminal lumbar interbody fusion (TLIF), and anterior lumbar interbody fusion (ALIF) cages designed for surgical spinal stabilization.
These products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Black Widow Anterior Buttress Plate Ref K081770
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omni Surgical, L.P. have in the registry?
The registry currently lists 2 devices for Omni Surgical, L.P.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omni Surgical, L.P.'s devices?
Among its 2 most recently registered devices, Omni Surgical, L.P. has devices listed in FDA 510(k) (2 devices).
What risk classes do Omni Surgical, L.P.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Omni Surgical, L.P.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omni Surgical, L.P. in the registry?
The most recently registered devices listed for Omni Surgical, L.P. include BLACK WIDOW ANTERIOR BUTTRESS PLATE and STINGRAY CERVICAL CAGE; SHARK IMPLANT (PLIF); BULL SHARK IMPLANT(PLIF); TIGER IMPLANT (TLIF); GREAT WHITE IMPLANTS(ALIF).