Allen Medical Instruments Corp.
Country not established
- Devices
- 1
What Allen Medical Instruments Corp. makes
Allen Medical Instruments Corp. manufactures the GEMINI E, a medical device designed for use in surgical procedures, likely as a powered surgical instrument or energy device for tissue dissection or coagulation.
The GEMINI E is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Gemini E Ref K993623
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Allen Medical Instruments Corp. have in the registry?
The registry currently lists 1 device for Allen Medical Instruments Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Allen Medical Instruments Corp.'s devices?
Among its 1 most recently registered device, Allen Medical Instruments Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Allen Medical Instruments Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Allen Medical Instruments Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Allen Medical Instruments Corp. in the registry?
The most recently registered devices listed for Allen Medical Instruments Corp. include GEMINI E.