510(k) · Cleared
ClearedVX650
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Luneau Technology Operations · HKI Camera, Ophthalmic, Ac-Powered
Cleared on Jan 29, 2021 as substantially equivalent to K162067 (Luneau Sas, 2017) and 2 other predicates after a 176-day review. Its family tree reaches back 8 generations to 1995.
- Decided
- Jan 29, 2021
- Review
- 176 days
- Class
- Class II
- Product code
- HKI
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 8 generations to K941234 (1995). 34 ancestors in all, the oldest K810880 (1981). No later device cites it as a predicate yet.
- Root · 8 generations backK941234 Non-Mydriatic Retinal CameraCanon USA, Inc. · 1995
- 7 generations backK980246 Non-Mydriatic Retinal Camera, Model CR6-45NMCanon USA, Inc. · 1998
- 6 generations backK014274 Non-Mydriatic Fundus Camera, Model NM-1000Nidek, Inc. · 2002
- 5 generations backK023719 MP-1 Micro PerimeterNidek Technologies Srl · 2002
- 4 generations backK061768 MP-1 MicroperimeterNidek Technologies Srl · 2006
- 3 generations backK070231 ORIONNidek Technologies Srl · 2007
- 2 generations backK101935 Centervue Digital Retinography SystemCentervue S.P.A. · 2010
- 1 generation backK180306 NexyNext Sight Srl · 2018
- This deviceK202221 VX650Luneau Technology Operations · 2021
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −8 | K941234 | Non-Mydriatic Retinal Camera | Canon USA, Inc. | 1995 | — |
| −7 | K980246 | Non-Mydriatic Retinal Camera, Model CR6-45NM | Canon USA, Inc. | 1998 | — |
| −6 | K014274 | Non-Mydriatic Fundus Camera, Model NM-1000 | Nidek, Inc. | 2002 | — |
| −5 | K023719 | MP-1 Micro Perimeter | Nidek Technologies Srl | 2002 | — |
| −4 | K061768 | MP-1 Microperimeter | Nidek Technologies Srl | 2006 | — |
| −3 | K070231 | ORION | Nidek Technologies Srl | 2007 | — |
| −2 | K101935 | Centervue Digital Retinography System | Centervue S.P.A. | 2010 | — |
| −1 | K180306 | Nexy | Next Sight Srl | 2018 | — |
| 0 (this device) | K202221 | VX650 | Luneau Technology Operations | 2021 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1981 | 1 | 0 |
| 1991 | 1 | 0 |
| 1995 | 1 | 0 |
| 1996 | 1 | 0 |
| 1997 | 1 | 0 |
| 1998 | 2 | 0 |
| 1999 | 2 | 0 |
| 2001 | 2 | 0 |
| 2002 | 1 | 0 |
| 2003 | 2 | 0 |
| 2004 | 2 | 0 |
| 2005 | 1 | 0 |
| 2006 | 1 | 0 |
| 2008 | 1 | 0 |
| 2009 | 2 | 0 |
| 2010 | 1 | 0 |
| 2011 | 1 | 0 |
| 2012 | 1 | 0 |
| 2015 | 1 | 0 |
| 2017 | 1 | 0 |
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 HKI? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new HKI device
- #1 K253176 TearViewscore 12.7 · 5 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K162067 | VX130 Ophthalmic Diagnostic DeviceSummary page 5…K Device, Analysis, Anterior II: Segment Device Description: The VX650 is based on the VX130 (already cleared 510(k), number K162067) which is a combined wavefront aberrometer, corneal topographer, Scheimpflug pachymeter, non-contact tonometer and cataract scree… | 2017 |
| * | K180306 | NexySummary page 7…510(k) no. Holder cleared to fundus camera module Nexy Next Sight K180306 8 June 2018 CenterVue Digital CenterVue K101935 27 October Retinography… | 2018 |
| * | K101935 | Centervue Digital Retinography SystemSummary page 7…cleared to fundus camera module Nexy Next Sight K180306 8 June 2018 CenterVue Digital CenterVue K101935 27 October Retinography 2010 System DRS… | 2010 |
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.
What does this lineage say?
- The line of descent spans 26 years and passes through 6 companies; a new generation was cleared every 3.5 years on median.
- 2 of the 34 ancestors have a recall of any class.
How does its category compare?
All HKI devicesHKI Camera, Ophthalmic, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.
FDA decisions per year · HKI
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HKI
167in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HKI
1in 2018
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HKI
1in 2023
MAUDE reports naming product code HKI, 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 | 2 | — | 0 | 3 |
| 2008 | 5 | 29 | 0 | 1 |
| 2009 | 11 | 104 | 0 | 1 |
| 2010 | 6 | 140 | 0 | 0 |
| 2011 | 7 | 160 | 0 | 0 |
| 2012 | 5 | 179 | 1 | 2 |
| 2013 | 7 | 141 | 0 | 22 |
| 2014 | 4 | 135 | 0 | 3 |
| 2015 | 0 | — | 0 | 3 |
| 2016 | 4 | 146 | 1 | 66 |
| 2017 | 2 | — | 1 | 20 |
| 2018 | 6 | 71 | 1 | 14 |
| 2019 | 4 | 73 | 0 | 0 |
| 2020 | 5 | 182 | 0 | 5 |
| 2021 | 4 | 155 | 0 | 3 |
| 2022 | 1 | — | 0 | 1 |
| 2023 | 5 | 259 | 0 | 1 |
| 2024 | 3 | 28 | 0 | 0 |
| 2025 | 4 | 167 | 0 | 0 |
| 2026 | 2 | — | 0 | — |
What is it indicated for?
The VX650 is a multi-function diagnostic device combining wavefront aberometer, corneal topographer, retro-illuminator, tonometer and pachymeter, indicated for: » Measuring the refraction of the eye giving both lower and higher order aberrations » Measuring the shape of the cornea * Retro-illumination imaging of the eye » Measuring the intraocular pressure without contacting the eye for glaucoma evaluation * Photographing the eye and taking images of the…
Read the full statement (119 words)
The VX650 is a multi-function diagnostic device combining wavefront aberometer, corneal topographer, retro-illuminator, tonometer and pachymeter, indicated for:
» Measuring the refraction of the eye giving both lower and higher order aberrations
» Measuring the shape of the cornea
* Retro-illumination imaging of the eye
» Measuring the intraocular pressure without contacting the eye for glaucoma evaluation
* Photographing the eye and taking images of the eye to evaluate the thickness of the central cornea
* Full cornea thickness map
* Scheimpflug imaging
* Anterior chamber imaging
* Pupil Image
* Image of the cornea relative to the iris
» Automatic eye-fundus camera intended for taking digital images of a human retina without the use of a mydriatic agent
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/K202221 · printed Nov 6, 2026
Cite this page
510(k) Report. “K202221: VX650.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K202221
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026