Trimed Systems, Inc.
Country not established
- Devices
- 1
What Trimed Systems, Inc. makes
Trimed Systems, Inc. develops the TRIMED PLAN software, version 2.2, a planning tool designed for medical procedures, likely in radiation therapy or surgical planning.
The TRIMED PLAN software is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Trimed Plan, Version 2.2 Ref K031088
510(k) 510(k)
Frequently asked questions
How many devices does Trimed Systems, Inc. have in the registry?
The registry currently lists 1 device for Trimed Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Trimed Systems, Inc.'s devices?
Among its 1 most recently registered device, Trimed Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Trimed Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Trimed Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Trimed Systems, Inc. in the registry?
The most recently registered devices listed for Trimed Systems, Inc. include TRIMED PLAN, VERSION 2.2.