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FDA PMA

Lens, intraocular, phakic

PMA Number: P030016 · 2026-03-04

ApplicantSTAAR Surgical Company
Decision Date2026-03-04
PMA NumberP030016
Product CodeMTA
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeOP

Device Summary

Lens, intraocular, phakic is the device name listed in this FDA 510(k) record. The listed applicant is STAAR Surgical Company. It received FDA 510(k) clearance on 2026-03-04. The device is classified under product code MTA. It was reviewed by the OP advisory panel.

Frequently Asked Questions

What is the Lens, intraocular, phakic?

Lens, intraocular, phakic is a medical device that received FDA 510(k) clearance on 2026-03-04. The listed applicant is STAAR Surgical Company.

When did Lens, intraocular, phakic receive FDA 510(k) clearance?

The clearance date for Lens, intraocular, phakic can be found in the official FDA records.

Who is the listed applicant for Lens, intraocular, phakic?

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

What is the FDA product code for Lens, intraocular, phakic?

The FDA product code for Lens, intraocular, phakic is MTA.

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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