Medical Device Manufacturer · US , Mchenry , IL

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

7 submissions · 7 cleared · Since 1981

7

Total

7

Cleared

0

Denied

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

6 devices

1-6 of 6

Cleared Mar 09, 1983

Ophthalmic · 33d

Cleared Dec 02, 1981

KOI BLUE FIELD ENTOPTOSCOPE

Ophthalmic · 61d

Cleared Sep 21, 1981

KOI DIAMOND KNIFE

Ophthalmic · 24d

Cleared Aug 18, 1981

KOI LACREMAL HOOK & DILATOR

Ophthalmic · 25d

Cleared Jul 28, 1981

KOI LACRIMAL INTUBATION SYSTEM

Ophthalmic · 11d

Cleared Jul 28, 1981

Ophthalmic · 11d