Medical Device Manufacturer · KR , Seoul

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

3 submissions · 3 cleared · Since 2015

3

Total

3

Cleared

0

Denied

INTEROJO, Inc. has 3 FDA 510(k) cleared medical devices. Based in Seoul, KR.

Last cleared in 2022. Active since 2015. Primary specialty: Ophthalmic.

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

FDA 510(k) cleared devices by INTEROJO, Inc.

3 devices

1-3 of 3

Cleared Oct 04, 2022

POLYVUE (polymacon) Soft (hydrophilic) Contact Lens, POLYVUE COLOR...

Ophthalmic · 132d

Cleared Apr 08, 2016

Clalen 54 (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear,...

Ophthalmic · 100d

Cleared Mar 12, 2015

I-55 (methafilcon A) Soft (hydrophilic) Contact Lenses for Daily Wear

Ophthalmic · 168d