510(k) · Cleared
ClearedEntry Site Alignment System Model # CX9626
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Bausch & Lomb, Inc. · NGY Cannula, Trocar, Ophthalmic
Cleared on Oct 2, 2001 after a 63-day review. The FDA summary names its predicate without a number.
- Decided
- Oct 2, 2001
- Review
- 63 days
- Class
- Class I
- Product code
- NGY
- Recalls
- None
- Predicates
- 0
The FDA summary names its predicate without a number.
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in NGY? 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
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | Alcon/Grieshaber Trocar Cannula Set Named without a submission number |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
How does its category compare?
All NGY devicesNGY Cannula, Trocar, Ophthalmic: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · NGY
FDA has decided no NGY device since 2007.
Median 510(k) review, days · NGY
Too few NGY 510(k)s in any year since 2007 to give a median.
Recalls per year · NGY
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NGY
20in 2025
MAUDE reports naming product code NGY, 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 | — | 1 | 1 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 2 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 4 |
| 2012 | 0 | — | 0 | 1 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 16 |
| 2016 | 0 | — | 0 | 64 |
| 2017 | 0 | — | 0 | 46 |
| 2018 | 0 | — | 0 | 25 |
| 2019 | 0 | — | 0 | 15 |
| 2020 | 0 | — | 2 | 9 |
| 2021 | 0 | — | 0 | 7 |
| 2022 | 0 | — | 0 | 10 |
| 2023 | 0 | — | 0 | 32 |
| 2024 | 0 | — | 0 | 14 |
| 2025 | 0 | — | 1 | 20 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The ESA is a hand-held surgical instrument intended for use as a trocar/cannula for establishing an entry site conduit for passing ophthalmic instruments/accessories used to perform posterior ophthalmic surgical procedures.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K012435 · printed Nov 4, 2026
Cite this page
510(k) Report. “K012435: Entry Site Alignment System Model # CX9626.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K012435
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
- Page last updated Nov 3, 2026