M.E.R. Surgical Co.
Country not established
- Devices
- 2
What M.E.R. Surgical Co. makes
M.E.R. Surgical Co. manufactures surgical instrument systems, including the OMNI Instrument System, designed for use in minimally invasive and open surgical procedures. These systems are intended to assist in tissue manipulation, dissection, and retraction during various surgical applications.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
M. E. R. Surgical Co. Omin Instrument System Ref K951424
510(k) 510(k)M.E.R. Surgical Co. Omni Instrument System Ref K944309
510(k) 510(k)
Frequently asked questions
How many devices does M.E.R. Surgical Co. have in the registry?
The registry currently lists 2 devices for M.E.R. Surgical Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list M.E.R. Surgical Co.'s devices?
Among its 2 most recently registered devices, M.E.R. Surgical Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do M.E.R. Surgical Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for M.E.R. Surgical Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from M.E.R. Surgical Co. in the registry?
The most recently registered devices listed for M.E.R. Surgical Co. include M. E. R. SURGICAL CO. OMIN INSTRUMENT SYSTEM and M.E.R. SURGICAL CO. OMNI INSTRUMENT SYSTEM.