Neoptx, Inc.
Country not established
- Devices
- 1
What Neoptx, Inc. makes
Neoptx, Inc. manufactures the OPTX 20/20, a device designed for low-level light therapy applications, likely targeting visual or ocular health.
The company’s portfolio is regulated under Class I medical devices in the US, with the OPTX 20/20 listed via FDA 510(k) clearance. The company is headquartered in the United States.
Catalogue
Optx 20/20 Ref K953413
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Neoptx, Inc. have in the registry?
The registry currently lists 1 device for Neoptx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Neoptx, Inc.'s devices?
Among its 1 most recently registered device, Neoptx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Neoptx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Neoptx, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Neoptx, Inc. in the registry?
The most recently registered devices listed for Neoptx, Inc. include OPTX 20/20.