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Anterior Chamber Intraocular Lens Model 120UV

FDA PMA

Class III (US FDA PMA)

PMA P880090

by Bausch & Lomb, Inc.

Identity

Trade Name
MODEL 120UV ANTERIOR CHAMBER INTRAOCULAR LENS FDA PMA
Generic Name
intraocular lens FDA PMA

Identifiers

PMA Number
P880090 FDA PMA
FDA Product Code
HQL FDA PMA

Classification

Device Class
Class III FDA PMA
Legislation / Framework
21 CFR Part 886.3600 FDA PMA
Regulation Number
886.3600 FDA PMA
Advisory Committee
Ophthalmic FDA PMA
FDA Decision
APPR Approved FDA PMA

An anterior chamber intraocular lens is a medical device implanted in the eye to replace the natural lens. This device, Model 120UV, is designed for ophthalmic use as a generic intraocular lens.

Supplied by Bausch & Lomb, Inc., it is a Class III device with FDA PMA approval (P880090, product code HQL). It is intended for use in ophthalmic surgical settings and is not described as sterile, single-use, or MRI safe in the provided data.

Frequently asked questions

What type of device is the Anterior Chamber Intraocular Lens Model 120UV?

It is an anterior chamber intraocular lens, which is a type of intraocular lens implanted in the anterior chamber of the eye to replace the natural lens, as defined by its generic name and device type in the specifications.

Who manufactures the Model 120UV intraocular lens?

The device is manufactured by Bausch & Lomb, Inc., as stated in the manufacturer and applicant fields of the device data.

What regulatory authorization does the Model 120UV have?

The device has FDA PMA authorization, with PMA number P880090, as indicated in the AUTHORIZATIONS and pma_number fields.

This description and any FAQs above were generated automatically from registry data and have not been verified by the manufacturer or by deviCERTS. Always check the official registry entry and the manufacturer's instructions for use before relying on them.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_PMA

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Manufacturer

Manufacturer
Bausch & Lomb, Inc.

Sources (1)

  • FDA PMA P880090 24 fields · synced Sep 18, 2026