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 spherical (lotrafilcon a) soft contact lenses with wetting agent (l% copolymer 845) in package saline, and the addition of descriptive text for symbols appearing on the cartons, except the rx symbol used for "prescription use," as well as the trade name changes to all the lotrafilcon a lens designs. The device, as modified, will be marketed under the following trade names: spherical - air optix night & day aqua; toric - air optix night & day aqua astigmatism; multifocal - air optix night & day aqua multifocal; and multifocal toric - air optix night & day aqua multifocal toric and is indicated for the following:air optixc night & day aqua (lotrafilcon a) 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 who have 1. 50 diopters or less of astigmatism. Air optix night & day aqua for astigmatism (lotrafilcon a) soft contact lenses are indicated for the optical correction of refractive ametropia (myopia and hyperopia) in phakic or aphakic persons with non-diseased eyes who have 6. 00 diopters (d) or less of astigmatism. Air optix night & day aqua multifocal (lotrafilcon a) 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 require a readingaddition of +4. 00 diopters (d) or less and who have 1. 50 diopters or less of astigmatism... (see approval order for additional statement detial)
| Device | AIR OPTIX NIGHT & DAY AQUA (LOTRAFILCON A) SOFT CONTACT LENSES |
| Classification Name | Lenses, Soft Contact, Extended Wear |
| Generic Name | Lenses, Soft Contact, Extended Wear |
| Applicant | Alcon Laboratories, Inc. |
| Date Received | 2011-06-06 |
| Decision Date | 2011-11-02 |
| PMA | P010019 |
| Supplement | S025 |
| 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 |