Pain Concepts, Inc.
Country not established
- Devices
- 1
What Pain Concepts, Inc. makes
Pain Concepts, Inc. manufactures the DeKompressor Percutaneous Lumbar Discectomy Probe, a device used for minimally invasive removal of herniated or bulging disc material in the lumbar spine.
The DeKompressor Percutaneous Lumbar Discectomy Probe 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
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pain Concepts, Inc. have in the registry?
The registry currently lists 1 device for Pain Concepts, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pain Concepts, Inc.'s devices?
Among its 1 most recently registered device, Pain Concepts, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Pain Concepts, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Pain Concepts, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Pain Concepts, Inc. in the registry?
The most recently registered devices listed for Pain Concepts, Inc. include DEKOMPRESSOR PERCUTANEOUS LUMBAR DISCECTOMY PROBE.