This article is more than 5 years old. Information may no longer be current.

Ophthalmic Imaging Systems receives 510(k) clearance to market portable imaging device

Add topic to email alerts

Receive an email when new articles are posted on

Please provide your email address to receive an email when new articles are posted on .

Subscribe

Added to email alerts

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

Back to Healio

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

Back to Healio

SACRAMENTO, Calif. — The U.S. Food and Drug Administration has granted Ophthalmic Imaging Systems 510(k) market clearance for its OIS EyeScan portable imaging device, the company announced in a press release.

Capable of imaging both the anterior and posterior segments from a chin rest, from a slit lamp adaptor or as a handheld device, the OIS EyeScan is powered by the company's OIS WinStation Software, which is fully integrated with its OIS Symphony Image Management Solution, the release said.

"The OIS EyeScan is already highly anticipated among our customers, and we are looking forward to delivering this device to the market," Gil Allon, CEO of OIS, said in the release. "The EyeScan brings an entirely new level of versatility to ophthalmologists' offices and is unlike any other single diagnostic imaging device ever released."