This medical device record is a pma supplement. A supplement may have changed the device description/function or indication from that approved in the original pma. Be sure to look at the original pma record for more information.
Approval for a trade name change to the (lotrafilcon b) soft contact lenses with wetting agent in package saline. The device, as modified, will be marketed under the trade name ciba vision air optix aqua (lotrafilcon b) and is indicated for the following: ciba vision air optix aqua (lotrafilcon b) spherical soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes with up to approximately 1. 50 diopters of astigmatism that does not interfere with visual acuity. Ciba vision air optix aqua (lotrafilcon b) toric soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes with up to 6. 00 diopters (d) or less of astigmatism. Ciba vision air optix aqua (lotrafilcon b) multifocal soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) and/or presbyopia in phakic or aphakic persons with non-diseased eyes who may required a reading addition of +3. 00 diopters (d) or less and who may have up to approximately 1. 50 diopters of astigmatism. Ciba vision air optix aqua (lotrafilcon b) multifocal toric soft contact lenses are indicated for the optical correction of refractive ametropia (myopia, hyperopia, astigmatism, and presbyopia) in phakic or aphakic persons with non-diseased eyes. The lenses may be worn by persons who have 10. 00 diopters (d) or less of refractive and/or corneal astigmatism. The lenses may be prescribed for daily wear or extended wear for up to 6 nights of continuous wear with removal for disposal, or cleaning and disinfection (chemical, not heat) prior to reinsertion, as recommended by the eye care professional.
Device | CIBA VISION AIR OPTIX AQUA (LOTRAFILCON B) SOFT CONTACT LENSES |
Classification Name | Lenses, Soft Contact, Extended Wear |
Generic Name | Lenses, Soft Contact, Extended Wear |
Applicant | Alcon Laboratories, Inc. |
Date Received | 2011-03-01 |
Decision Date | 2011-09-09 |
PMA | P010019 |
Supplement | S021 |
Product Code | LPM |
Advisory Committee | Ophthalmic |
Supplement Type | Normal 180 Day Track No User Fee |
Supplement Reason | Labeling Change - Indications/instructions/shelf Life/tradename |
Expedited Review | No |
Combination Product | No |
Applicant Address | Alcon Laboratories, Inc. 6201 South Freeway fort Worth, TX 76134-2099 |
Supplement Number | Date | Supplement Type |
---|---|---|
P010019 | Original Filing | |
S083 | 2022-06-09 | 30-day Notice |
S082 | ||
S081 | 2021-12-17 | 30-day Notice |
S080 | 2021-08-31 | 30-day Notice |
S079 | 2021-08-16 | 30-day Notice |
S078 | 2021-06-04 | Normal 180 Day Track No User Fee |
S077 | 2020-11-17 | 30-day Notice |
S076 | 2020-02-18 | 30-day Notice |
S075 | 2019-12-23 | 30-day Notice |
S074 | 2019-11-13 | 30-day Notice |
S073 | 2019-08-02 | 30-day Notice |
S072 | ||
S071 | 2019-02-21 | 30-day Notice |
S070 | 2018-11-27 | 30-day Notice |
S069 | ||
S068 | 2018-07-31 | 30-day Notice |
S067 | 2018-07-13 | 30-day Notice |
S066 | 2018-06-27 | 30-day Notice |
S065 | 2018-04-30 | 30-day Notice |
S064 | 2018-03-22 | 30-day Notice |
S063 | 2018-02-02 | 30-day Notice |
S062 | 2017-12-18 | Real-time Process |
S061 | 2017-10-17 | 30-day Notice |
S060 | 2017-09-27 | 30-day Notice |
S059 | 2017-08-29 | 30-day Notice |
S058 | 2017-08-28 | 30-day Notice |
S057 | ||
S056 | 2017-08-09 | 30-day Notice |
S055 | 2017-06-12 | 30-day Notice |
S054 | 2017-03-24 | 30-day Notice |
S053 | 2017-01-23 | 135 Review Track For 30-day Notice |
S052 | 2016-08-12 | 30-day Notice |
S051 | 2016-06-01 | 30-day Notice |
S050 | 2016-04-22 | Normal 180 Day Track |
S049 | 2016-03-11 | 30-day Notice |
S048 | 2016-03-01 | 30-day Notice |
S047 | 2016-02-26 | 30-day Notice |
S046 | 2016-02-16 | 30-day Notice |
S045 | 2016-02-09 | 30-day Notice |
S044 | 2016-01-28 | 30-day Notice |
S043 | 2015-12-21 | 30-day Notice |
S042 | 2015-11-12 | 30-day Notice |
S041 | 2015-09-21 | 30-day Notice |
S040 | 2015-07-30 | 30-day Notice |
S039 | 2015-05-01 | 30-day Notice |
S038 | 2015-04-08 | 30-day Notice |
S037 | 2015-03-03 | 30-day Notice |
S036 | 2013-11-12 | 30-day Notice |
S035 | 2013-08-02 | 30-day Notice |
S034 | 2012-09-27 | 30-day Notice |
S033 | 2012-07-10 | 30-day Notice |
S032 | 2012-05-04 | 30-day Notice |
S031 | 2012-04-23 | 30-day Notice |
S030 | 2012-04-16 | 30-day Notice |
S029 | 2012-02-01 | 30-day Notice |
S028 | 2011-12-14 | Normal 180 Day Track No User Fee |
S027 | 2011-12-12 | 30-day Notice |
S026 | 2011-09-30 | 30-day Notice |
S025 | 2011-06-06 | Normal 180 Day Track No User Fee |
S024 | 2011-04-21 | 30-day Notice |
S023 | 2011-04-13 | 30-day Notice |
S022 | 2011-03-25 | 135 Review Track For 30-day Notice |
S021 | 2011-03-01 | Normal 180 Day Track No User Fee |
S020 | 2011-02-14 | 30-day Notice |
S019 | 2010-08-09 | 30-day Notice |
S018 | 2010-08-06 | 30-day Notice |
S017 | 2010-06-29 | 30-day Notice |
S016 | ||
S015 | 2010-05-05 | 30-day Notice |
S014 | 2010-03-03 | 30-day Notice |
S013 | 2010-03-02 | 30-day Notice |
S012 | ||
S011 | 2008-08-25 | Normal 180 Day Track No User Fee |
S010 | 2008-07-07 | 30-day Notice |
S009 | 2008-04-07 | Normal 180 Day Track No User Fee |
S008 | 2007-12-17 | Real-time Process |
S007 | 2007-09-14 | Normal 180 Day Track No User Fee |
S006 | 2007-04-02 | Normal 180 Day Track No User Fee |
S005 | 2006-11-20 | 30-day Notice |
S004 | 2006-08-22 | Real-time Process |
S003 | 2004-06-08 | Normal 180 Day Track |
S002 | 2003-02-24 | Real-time Process |
S001 | 2002-04-05 | Normal 180 Day Track |