Opti-Med Electronics
Country not established
- Devices
- 1
What Opti-Med Electronics makes
Opti-Med Electronics manufactures digital averaging tonometers, which are devices used to measure intraocular pressure in the eye for glaucoma assessment and monitoring.
The company’s products are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Digital Averaging Tonometer Ref K945972
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Opti-Med Electronics have in the registry?
The registry currently lists 1 device for Opti-Med Electronics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Opti-Med Electronics's devices?
Among its 1 most recently registered device, Opti-Med Electronics has devices listed in FDA 510(k) (1 device).
What risk classes do Opti-Med Electronics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Opti-Med Electronics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Opti-Med Electronics in the registry?
The most recently registered devices listed for Opti-Med Electronics include DIGITAL AVERAGING TONOMETER.