510(k) · Cleared
ClearedD.O.R.C. Vfi/Vfe System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dutch Ophthalmic USA, Inc. · KYG Device, Irrigation, Ocular Surgery
Cleared on Apr 15, 1996 after a 175-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 12 later devices descend from it.
- Decided
- Apr 15, 1996
- Review
- 175 days
- Class
- Class I
- Product code
- KYG
- Recalls
- None
- Predicates
- 0
12 later devices descend from it, 1 citing it directly.
- This deviceK954842 D.O.R.C. Vfi/Vfe SystemDutch Ophthalmic USA, Inc. · 1996
- Descendant · cites it directly · 11 of its ownK050716 Iscience Surgical ViscoinjectorIscience Surgical Corporation · 2005
- Descendant · 2 generations on · 10 of its ownK132494 Viscoelastic InjectorSight Sciences, Inc. · 2013
- Descendant · 3 generations on · 9 of its ownK143205 Viscoelastic InjectorSight Sciences, Inc. · 2014
- Descendant · 4 generations on · 8 of its ownK171905 VISCO 360 Viscosurgical SystemSight Sciences, Inc. · 2017
- Descendant · 5 generations on · 6 of its ownK173332 OMNI Surgical SystemSight Sciences, Inc. · 2017
Showing 5 of 12 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 12 · See all- K050716Iscience Surgical ViscoinjectorIscience Surgical Corporation · 2005 · cites it directly11descendants
- K132494Viscoelastic InjectorSight Sciences, Inc. · 2013 · 2 generations on10descendants
- K143205Viscoelastic InjectorSight Sciences, Inc. · 2014 · 3 generations on9descendants
- K171905VISCO 360 Viscosurgical SystemSight Sciences, Inc. · 2017 · 4 generations on8descendants
- K173332OMNI Surgical SystemSight Sciences, Inc. · 2017 · 5 generations on6descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K954842 | D.O.R.C. Vfi/Vfe System | Dutch Ophthalmic USA, Inc. | 1996 | — |
| +1 | K050716 | Iscience Surgical Viscoinjector | Iscience Surgical Corporation | 2005 | — |
| +2 | K132494 | Viscoelastic Injector | Sight Sciences, Inc. | 2013 | — |
| +3 | K143205 | Viscoelastic Injector | Sight Sciences, Inc. | 2014 | — |
| +4 | K171905 | VISCO 360 Viscosurgical System | Sight Sciences, Inc. | 2017 | — |
| +5 | K173332 | OMNI Surgical System | Sight Sciences, Inc. | 2017 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 0 |
| 2013 | 1 | 0 |
| 2014 | 1 | 0 |
| 2017 | 2 | 0 |
| 2020 | 1 | 0 |
| 2021 | 2 | 0 |
| 2022 | 1 | 0 |
| 2023 | 1 | 0 |
| 2025 | 1 | 0 |
| 2026 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in KYG? 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?
FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.
What descends from it? (12)
See all 121 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K050716 | Iscience Surgical Viscoinjector | 2005 | 11 |
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.
What does this lineage say?
- Of its descendants, K050716 (Iscience Surgical Corporation, 2005) has gone furthest, with 11 descendants of its own.
How does its category compare?
All KYG devicesKYG Device, Irrigation, Ocular Surgery: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KYG
FDA has decided no KYG device since 2007.
Median 510(k) review, days · KYG
Too few KYG 510(k)s in any year since 2007 to give a median.
Recalls per year · KYG
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KYG
72in 2025
MAUDE reports naming product code KYG, 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 | — | 4 | 103 |
| 2008 | 0 | — | 0 | 61 |
| 2009 | 0 | — | 0 | 50 |
| 2010 | 0 | — | 2 | 127 |
| 2011 | 0 | — | 0 | 81 |
| 2012 | 0 | — | 0 | 332 |
| 2013 | 0 | — | 0 | 242 |
| 2014 | 0 | — | 0 | 258 |
| 2015 | 0 | — | 0 | 79 |
| 2016 | 0 | — | 0 | 14 |
| 2017 | 0 | — | 0 | 10 |
| 2018 | 0 | — | 0 | 10 |
| 2019 | 0 | — | 0 | 13 |
| 2020 | 0 | — | 0 | 8 |
| 2021 | 0 | — | 0 | 19 |
| 2022 | 0 | — | 0 | 20 |
| 2023 | 0 | — | 1 | 23 |
| 2024 | 0 | — | 0 | 81 |
| 2025 | 0 | — | 0 | 72 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K954842 · printed Nov 5, 2026
Cite this page
510(k) Report. “K954842: D.O.R.C. Vfi/Vfe System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K954842
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026