Medical Device Manufacturer · US , Mchenry , IL

Koi, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 1981

Total

Cleared

Denied

Koi, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 7 cleared submissions from 1981 to 1986. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Koi, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Koi, Inc.

7 devices

1-7 of 7