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Intraocular Pressure Lowering Implant

FDA product code OGO · Class 3 · Unknown

9
Registered devices
2,671
Adverse events
4
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-08-28Alcon Research, LTD.Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial
2018-08-28Alcon Research, LTD.Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial
2018-08-28Alcon Research, LTD.Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial
2018-08-28Alcon Research, LTD.Analysis of the completed dataset from the COMPASS-XT long-term study showed that the CyPass Micro-Stent group experienced statistically significant endothelial

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.