510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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OGOClass III

Intraocular Pressure Lowering Implant

Unknown
FDA source (opens on fda.gov)

OGO is the FDA product code for Intraocular Pressure Lowering Implant, a class III device type. FDA's definition for this code reads: "An intraocular pressure lowering implant is a device intended to reduce intraocular pressure when implanted in eyes which have not failed conventional medical and surgical treatment". As of , FDA records hold no 510(k) clearances under this code and 4 recalls.

Classification record

Product code
OGO
Device name
Intraocular Pressure Lowering Implant
FDA definition
An intraocular pressure lowering implant is a device intended to reduce intraocular pressure when implanted in eyes which have not failed conventional medical and surgical treatment.
Device class
Class III
Review panel
Unknown
Submission type
PMA
Implant
Yes
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
0
Ingested recalls
4

Companies listing this code with FDA

Companies whose registered establishments list this code