Encision Incorporated
Country not established
- Devices
- 1
What Encision Incorporated makes
Encision Incorporated manufactures monopolar laparoscopic instruments and associated accessories designed for minimally invasive surgical procedures. These tools are intended for use in abdominal and pelvic surgeries, enabling precise tissue dissection and coagulation.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These instruments are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Encision Incorporated have in the registry?
The registry currently lists 1 device for Encision Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Encision Incorporated's devices?
Among its 1 most recently registered device, Encision Incorporated has devices listed in FDA 510(k) (1 device).
What risk classes do Encision Incorporated's devices fall under?
Among its 1 most recently registered device, the classes recorded for Encision Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Encision Incorporated in the registry?
The most recently registered devices listed for Encision Incorporated include Encision AEM Monopolar Laparoscopic Instruments and Accessories.