Iotec Industries
Country not established
- Devices
- 1
What Iotec Industries makes
Iotec Industries manufactures surgical trocars and flexible cannulas, designed for minimally invasive procedures to facilitate instrument insertion and tissue access.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Iotec Trocar And Flexible Cannula Ref K970888
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Iotec Industries have in the registry?
The registry currently lists 1 device for Iotec Industries. Devices recorded under merged duplicate company entries are counted once.
Which registries list Iotec Industries's devices?
Among its 1 most recently registered device, Iotec Industries has devices listed in FDA 510(k) (1 device).
What risk classes do Iotec Industries's devices fall under?
Among its 1 most recently registered device, the classes recorded for Iotec Industries's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Iotec Industries in the registry?
The most recently registered devices listed for Iotec Industries include IOTEC TROCAR AND FLEXIBLE CANNULA.