PMA · Approved
Recalled · 2006Acrysof Restor Apodized Diffractive Optic Posterior Chamber Iol
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Alcon Research, Ltd. · MFK Lens, Multifocal Intraocular
Approved on Mar 21, 2005 through premarket approval, which rests on the device’s own clinical evidence after a 336-day review. It has been recalled 2 times.
- Decided
- Mar 21, 2005
- Review
- 336 days
- Class
- Class III
- Product code
- MFK
- Recalls
- 2
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
P040020 has 118 supplements since 2005: changes to the approved device, its labelling or its manufacturing, each approved separately.
PMA supplements approved per year
View FIG. 1 as a table
| Year | Supplements approved |
|---|---|
| 2005 | 1 |
| 2006 | 1 |
| 2007 | 4 |
| 2008 | 6 |
| 2009 | 9 |
| 2010 | 7 |
| 2011 | 10 |
| 2012 | 5 |
| 2013 | 6 |
| 2014 | 4 |
| 2015 | 2 |
| 2016 | 7 |
| 2017 | 9 |
| 2018 | 13 |
| 2019 | 6 |
| 2020 | 3 |
| 2021 | 5 |
| 2022 | 4 |
| 2023 | 2 |
| 2024 | 4 |
| 2025 | 6 |
| 2026 | 4 |
Sources: FDA PMA database (decision fields and supplements), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in MFK? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
Does it have a predicate?
PMA decisions do not claim a predicate device.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Dec 14, 2006 | Not classified | Z-0430-2007 | Other | Intraocular lenses exposed to extreme temperatures while in storage. |
| Dec 14, 2006 | Not classified | Z-0429-2007 | Other | Intraocular lenses exposed to extreme temperatures while in storage. |
No ancestor or descendant has a Class I recall.
How does its category compare?
All MFK devicesMFK Lens, Multifocal Intraocular: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MFK
17so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · MFK
Too few MFK 510(k)s in any year since 2007 to give a median.
Recalls per year · MFK
No recall names MFK since 2007.
Adverse event reports per year · MFK
717in 2025
MAUDE reports naming product code MFK, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 13 | — | 0 | 35 |
| 2008 | 12 | — | 0 | 420 |
| 2009 | 14 | — | 0 | 586 |
| 2010 | 9 | — | 0 | 601 |
| 2011 | 10 | — | 0 | 584 |
| 2012 | 9 | — | 0 | 308 |
| 2013 | 9 | — | 0 | 296 |
| 2014 | 5 | — | 0 | 308 |
| 2015 | 3 | — | 0 | 708 |
| 2016 | 11 | — | 0 | 731 |
| 2017 | 12 | — | 0 | 613 |
| 2018 | 12 | — | 0 | 629 |
| 2019 | 8 | — | 0 | 683 |
| 2020 | 4 | — | 0 | 912 |
| 2021 | 8 | — | 0 | 1,205 |
| 2022 | 8 | — | 0 | 1,265 |
| 2023 | 6 | — | 0 | 1,047 |
| 2024 | 11 | — | 0 | 859 |
| 2025 | 14 | — | 0 | 717 |
| 2026 | 17 | — | 0 | — |
https://510kreport.com/device/P040020 · printed Nov 6, 2026
Cite this page
510(k) Report. “P040020: Acrysof Restor Apodized Diffractive Optic Posterior Chamber Iol.” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P040020
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026