PMA · Approved
Recalled · Class II · 2026Visian Icl (Implantable Collamer Lens)
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
STAAR Surgical Company · MTA Lens, Intraocular, Phakic
Approved on Dec 22, 2005 through premarket approval, which rests on the device’s own clinical evidence after a 959-day review. It has been recalled 8 times.
- Decided
- Dec 22, 2005
- Review
- 959 days
- Class
- Class III
- Product code
- MTA
- Recalls
- 8
PMA approvals rest on their own clinical evidence and do not claim a predicate, so this family tree starts here.
P030016 has 45 supplements since 2008: 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 |
|---|---|
| 2008 | 7 |
| 2009 | 3 |
| 2010 | 4 |
| 2011 | 3 |
| 2012 | 1 |
| 2013 | 1 |
| 2014 | 2 |
| 2015 | 2 |
| 2017 | 5 |
| 2018 | 1 |
| 2019 | 5 |
| 2020 | 1 |
| 2021 | 1 |
| 2022 | 3 |
| 2024 | 2 |
| 2025 | 3 |
| 2026 | 1 |
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 MTA? 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 |
|---|---|---|---|---|
| Jan 21, 2026 | Class II | Z-1480-2026 | Process control | Toric Implantable Collamer for correction/reduction of myopia in phakic eyes with astigmatism were labeled as 12.1 mm length but are 12.6 mm length lenses, so there is the potential for excessive vault, which may cause: Significant… |
| Sep 29, 2023 | Class II | Z-0464-2024 | Software design (manufacturing process) | Their is a potential that intraocular implant devices may not meet specifications. |
| Sep 29, 2023 | Class II | Z-0465-2024 | Software design (manufacturing process) | Their is a potential that intraocular implant devices may not meet specifications. |
| Sep 29, 2023 | Class II | Z-0466-2024 | Software design (manufacturing process) | Their is a potential that intraocular implant devices may not meet specifications. |
| Sep 29, 2023 | Class II | Z-0467-2024 | Software design (manufacturing process) | Their is a potential that intraocular implant devices may not meet specifications. |
| Sep 29, 2023 | Class II | Z-0469-2024 | Software design (manufacturing process) | Their is a potential that intraocular implant devices may not meet specifications. |
| Sep 29, 2023 | Class II | Z-0474-2024 | Software design (manufacturing process) | Their is a potential that intraocular implant devices may not meet specifications. |
| Sep 29, 2023 | Class II | Z-0468-2024 | Software design (manufacturing process) | Their is a potential that intraocular implant devices may not meet specifications. |
The 5 latest of 8 recalls; the web page lists all.
No ancestor or descendant has a Class I recall.
How does its category compare?
All MTA devicesMTA Lens, Intraocular, Phakic: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · MTA
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MTA
Too few MTA 510(k)s in any year since 2007 to give a median.
Recalls per year · MTA
7in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MTA
655in 2025
MAUDE reports naming product code MTA, 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 | 0 | — | 0 | 4 |
| 2008 | 7 | — | 0 | 226 |
| 2009 | 3 | — | 0 | 601 |
| 2010 | 5 | — | 0 | 551 |
| 2011 | 4 | — | 0 | 311 |
| 2012 | 2 | — | 0 | 500 |
| 2013 | 1 | — | 0 | 696 |
| 2014 | 2 | — | 0 | 781 |
| 2015 | 2 | — | 0 | 1,279 |
| 2016 | 0 | — | 0 | 1,456 |
| 2017 | 5 | — | 0 | 1,796 |
| 2018 | 3 | — | 0 | 1,778 |
| 2019 | 6 | — | 0 | 1,236 |
| 2020 | 1 | — | 0 | 1,440 |
| 2021 | 1 | — | 0 | 2,063 |
| 2022 | 4 | — | 0 | 1,917 |
| 2023 | 0 | — | 7 | 2,076 |
| 2024 | 4 | — | 0 | 2,148 |
| 2025 | 2 | — | 0 | 655 |
| 2026 | 2 | — | 1 | — |
https://510kreport.com/device/P030016 · printed Nov 6, 2026
Cite this page
510(k) Report. “P030016: Visian Icl (Implantable Collamer Lens).” Lineage record from FDA PMA data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/P030016
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026