Stimwave Technologies Inc., Dba Stimq, LLC
Country not established
- Devices
- 1
What Stimwave Technologies Inc., Dba Stimq, LLC makes
Stimwave Technologies Inc. manufactures kits for implantable neurostimulation systems, including receiver, trial, spare lead, sterile revision, and SWAG (surgical access) kits, along with associated charger and accessory components.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit Ref K171366
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stimwave Technologies Inc., Dba Stimq, LLC have in the registry?
The registry currently lists 1 device for Stimwave Technologies Inc., Dba Stimq, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stimwave Technologies Inc., Dba Stimq, LLC's devices?
Among its 1 most recently registered device, Stimwave Technologies Inc., Dba Stimq, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Stimwave Technologies Inc., Dba Stimq, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Stimwave Technologies Inc., Dba Stimq, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stimwave Technologies Inc., Dba Stimq, LLC in the registry?
The most recently registered devices listed for Stimwave Technologies Inc., Dba Stimq, LLC include Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit.