FDA PMA

intraocular lens

PMA Number: P090022 · 2026-04-15

ApplicantLenstec, Inc.

Decision Date2026-04-15

PMA NumberP090022

Product CodeHQL

Device ClassClass 3

Medical SpecialtyO

Regulation Number21 CFR 8

Advisory CommitteeOP

Device Summary

intraocular lens is the device name listed in this FDA 510(k) record. The listed applicant is Lenstec, Inc.. It received FDA 510(k) clearance on 2026-04-15. The device is classified under product code HQL. It was reviewed by the OP advisory panel.

Frequently Asked Questions

What is the intraocular lens?

intraocular lens is a medical device that received FDA 510(k) clearance on 2026-04-15. The listed applicant is Lenstec, Inc..

When did intraocular lens receive FDA 510(k) clearance?

The clearance date for intraocular lens can be found in the official FDA records.

Who is the listed applicant for intraocular lens?

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

What is the FDA product code for intraocular lens?

The FDA product code for intraocular lens is HQL.

Related Clinical Trials

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Official Source

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