Minimal Invasive Therapy and Diagnostics, Inc.
Country not established
- Devices
- 1
What Minimal Invasive Therapy and Diagnostics, Inc. makes
Minimal Invasive Therapy and Diagnostics, Inc. manufactures the OPTIFIBER, a device designed for minimally invasive medical procedures, likely used in endoscopic or fiber-optic applications for diagnostic or therapeutic purposes.
The OPTIFIBER is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Optifiber Ref K914423
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Minimal Invasive Therapy and Diagnostics, Inc. have in the registry?
The registry currently lists 1 device for Minimal Invasive Therapy and Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Minimal Invasive Therapy and Diagnostics, Inc.'s devices?
Among its 1 most recently registered device, Minimal Invasive Therapy and Diagnostics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Minimal Invasive Therapy and Diagnostics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Minimal Invasive Therapy and Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Minimal Invasive Therapy and Diagnostics, Inc. in the registry?
The most recently registered devices listed for Minimal Invasive Therapy and Diagnostics, Inc. include OPTIFIBER.