INTEROJO, Inc. - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Eyereg Consulting, Inc. as regulatory consultant.
3 devices
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