PRESS RELEASE: Lenstec expands Softec HD Series With Approval of HDM (MICRO) Intraocular Lens

4/7/2016

Lenstec, Inc, a manufacturer of technologically advanced implantable lenses for correcting vision, today announced it has expanded its Softec HD product line with the Softec HDM, which was approved by the U.S. Food & Drug Administration in March..

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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

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Christ Church, Barbados BB17092
Tel: 246-420-6795
Fax: 246-420-6797

LENSTEC UK

LENSTEC (BARBADOS) INC.
LENSTEC HOUSE
UNIT 8, MARINER House
CALDER PARK
WAKEFIELD
West Yorkshire wf4 3fl
ENGLAND
TEL: +44 (0)1924 382 678
FAX:+44 (0)1924 850 454

EUROPEAN REGIONAL OFFICE

TRENCIANSKA 47
821 09 BRATISLAVA
SLOVAK REPUBLIC

TEL: 00421905798760

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
© 2016 Lenstec, Inc. All Rights Reserved. Lenstec, Softec, Softec HD, Tetraflex, SBL-3, and the Softec HD logo are registered trademarks of Lenstec, Inc.