Sterilemed, Inc.
Country not established
- Devices
- 1
What Sterilemed, Inc. makes
Sterilemed, Inc. manufactures reprocessed external fixation devices, which are used in orthopedic surgery to stabilize and support bone fractures or deformities externally.
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
Reprocessed External Fixation Device Ref K051957
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sterilemed, Inc. have in the registry?
The registry currently lists 1 device for Sterilemed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sterilemed, Inc.'s devices?
Among its 1 most recently registered device, Sterilemed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sterilemed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sterilemed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sterilemed, Inc. in the registry?
The most recently registered devices listed for Sterilemed, Inc. include REPROCESSED EXTERNAL FIXATION DEVICE.