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FDA PMA

Intraocular pressure lowering implant

PMA Number: P170043 · 2026-10-01

ApplicantGlaukos Corporation
Decision Date2026-10-01
PMA NumberP170043
Product CodeOGO
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOP

Device Summary

Intraocular pressure lowering implant is the device name listed in this FDA 510(k) record. The listed applicant is Glaukos Corporation. It received FDA 510(k) clearance on 2026-10-01. The device is classified under product code OGO. It was reviewed by the OP advisory panel.

Frequently Asked Questions

What is the Intraocular pressure lowering implant?

Intraocular pressure lowering implant is a medical device that received FDA 510(k) clearance on 2026-10-01. The listed applicant is Glaukos Corporation.

When did Intraocular pressure lowering implant receive FDA 510(k) clearance?

The clearance date for Intraocular pressure lowering implant can be found in the official FDA records.

Who is the listed applicant for Intraocular pressure lowering implant?

The FDA 510(k) record lists Glaukos Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Intraocular pressure lowering implant?

The FDA product code for Intraocular pressure lowering implant is OGO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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