Argus Biomedical Pty, Ltd.
Country not established
- Devices
- 1
What Argus Biomedical Pty, Ltd. makes
Argus Biomedical manufactures the ALPHACOR family of corneal inlays, including variants for aphakic (ALPHACOR-A) and phakic/pseudophakic eyes (ALPHACOR-P). These devices are designed to correct refractive errors by reshaping the cornea to improve vision without surgery.
The ALPHACOR inlays are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Argus Biomedical Pty, Ltd. have in the registry?
The registry currently lists 1 device for Argus Biomedical Pty, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Argus Biomedical Pty, Ltd.'s devices?
Among its 1 most recently registered device, Argus Biomedical Pty, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Argus Biomedical Pty, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Argus Biomedical Pty, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Argus Biomedical Pty, Ltd. in the registry?
The most recently registered devices listed for Argus Biomedical Pty, Ltd. include ALPHACOR; ALPHACOR-A (FOR AHAKIC EYES); ALPHACOR-P (FOR PHAKIC OR PSEUDOPHAKIC EYES).