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TECHNICAL SPECIFICATIONS
RESOURCES

ClearView 3 Multifocal IOL

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The ClearView 3 MIOL is now FDA approved!

The Lenstec ClearView 3 Multifocal IOL is a presbyopic lens that is intended to provide superior HD vision. It is a asymmetric segmented multifocal IOL (MIOL) that is designed to improve contrast sensitivity, minimize halos and glare, and provide superior near, intermediate and distance vision compared to other presbyopic IOLs.

The Lenstec ClearView 3 MIOL provides both surgeon and patient a very high level of confidence based on the manufacturing tolerances and the availability of 0.25 Diopter power increments.  This process enables Lenstec to manufacture the ClearView 3 to an industry leading ±0.11 Diopters of the intended power, allowing it to be distinguished as part of the Precision Series.    The ClearView 3 comes with a true 3.0 diopter sector-shaped add with a seamless transition zone between the distance and near segments.

Several prospective studies have been performed on the ClearView 3 with results identifying a high level of near, intermediate and distance vision, very limited amounts of visual side effects and extremely high patient satisfaction and spectacle independence ratings.  




World Headquarters

Lenstec, Inc.
1765 Commerce Ave. N.
St. Petersburg, FL 33716 USA
Tel: +1 727-571-2272
Fax: +1 727-571-1792



U.S. CUSTOMER SERVICE:
TEL: 1-866-536-7832
FAX: 1-866-536-3040

​Lenstec Barbados

Lenstec (Barbados) Inc.
Airport Commercial Centre
Pilgrim Road
Christ Church, Barbados BB17092
Tel: 246-420-6795
Fax: 246-420-6797



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LENSTEC UK

LENSTEC (BARBADOS) INC.
LENSTEC HOUSE
UNIT 8, MARINER House
CALDER PARK
WAKEFIELD

West Yorkshire wf4 3fl
ENGLAND
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TEL: +44 (0)1924 382 678
FAX:+44 (0)1924 850 454
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EUROPEAN REGIONAL OFFICE

TRENCIANSKA 47
821 09 BRATISLAVA
SLOVAK REPUBLIC

TEL: 00421905798760





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​INDICATION 
The Lenstec Softec Aspheric Posterior Chamber Intraocular Lens is intended for the replacement of the human crystalline lens following phacoemulsification cataract removal in adults over the age of 21. The lens is indicated for capsular bag placement.
CAUTION: Federal (U.S.) law restricts some of these devices to the sale by or on the order of a physician.
Lenstec, Inc. is an ISO 13485 company manufacturing CE Marked Products with additional registrations of several countries.
​DUNS: 807554100
© 2021 Lenstec, Inc. All Rights Reserved. Lenstec, Softec, Softec HD, Tetraflex, SBL-3, and the Softec HD logo are registered trademarks of Lenstec, Inc.