Retinapharma Technologies, Inc.
Country not established
- Devices
- 1
What Retinapharma Technologies, Inc. makes
Retinapharma Technologies, Inc. manufactures the TONOPACH Ultrasonic Tonometer/Pachymeter Model P-201, a device used to measure intraocular pressure and corneal thickness in ophthalmology.
The TONOPACH 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 Retinapharma Technologies, Inc. have in the registry?
The registry currently lists 1 device for Retinapharma Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Retinapharma Technologies, Inc.'s devices?
Among its 1 most recently registered device, Retinapharma Technologies, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Retinapharma Technologies, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Retinapharma Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Retinapharma Technologies, Inc. in the registry?
The most recently registered devices listed for Retinapharma Technologies, Inc. include TONOPACH ULTRASONIC TONOMETER/PACHYMETER MODEL P-201 (THE TONOPACH).