PMA de la FDA

Lens, intraocular, phakic

Número de PMA: P030028 · 2026-04-24

SolicitanteOphtec BV

Fecha de decisión2026-04-24

Número PMAP030028

Código de productoMTA

Clase del dispositivoClase 3

Especialidad médicaU

Comité asesorOP

Resumen del dispositivo

Lens, intraocular, phakic is the device name listed in this FDA 510(k) record. The listed applicant is Ophtec BV. It received FDA 510(k) clearance on 2026-04-24. The device is classified under product code MTA. It was reviewed by the OP advisory panel.

Preguntas frecuentes

What is the Lens, intraocular, phakic?

Lens, intraocular, phakic is a medical device that received FDA 510(k) clearance on 2026-04-24. The listed applicant is Ophtec BV.

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 Ophtec BV 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.

Ensayos clínicos relacionados

Los registros relacionados se emparejan automáticamente mediante nombres, códigos de producto u otros metadatos. Un emparejamiento no establece una relación clínica, científica, corporativa o regulatoria verificada; revise las fuentes oficiales enlazadas.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Fuente oficial

Ver en la base de datos de la FDA →

Datos procedentes de la API abierta de la FDA. Para obtener la información más actualizada y autoritativa, consulte siempre el registro oficial.