510(k) · Cleared
ClearedVS Tabletop Tonometer
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medimaging Integrated Solution, Inc. · HKX Tonometer, Ac-Powered
Cleared on Nov 8, 2023 as substantially equivalent to K181260 (Medimaging Integrated Solution, Inc (Miis), 2019) and 1 other predicate after a 329-day review. Its family tree reaches back 5 generations to 1995.
- Decided
- Nov 8, 2023
- Review
- 329 days
- Class
- Class II
- Product code
- HKX
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 5 generations to K943939 (1995). 8 ancestors in all, the oldest K871335 (1987). No later device cites it as a predicate yet.
- Root · 5 generations backK943939 Non-Contact Tonometer T-2Canon, Inc. · 1995
- 4 generations backK963079 Canon TX-10 TonometerCanon USA, Inc. · 1997
- 3 generations backK023816 Canon Full Auto Tonometer TX-FCanon, Inc.-Utsunomiya Optical Products Operation · 2002
- 2 generations backK111710 Full Auto Tonometer Model TX-20Canon Inc. -Medical Equipment Group · 2011
- 1 generation backK180820 Tono Vue Non-Contact TonometerCrystalvue Medical Corporation · 2018
- This deviceK223739 VS Tabletop TonometerMedimaging Integrated Solution, Inc. · 2023
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K943939 | Non-Contact Tonometer T-2 | Canon, Inc. | 1995 | — |
| −4 | K963079 | Canon TX-10 Tonometer | Canon USA, Inc. | 1997 | — |
| −3 | K023816 | Canon Full Auto Tonometer TX-F | Canon, Inc.-Utsunomiya Optical Products Operation | 2002 | — |
| −2 | K111710 | Full Auto Tonometer Model TX-20 | Canon Inc. -Medical Equipment Group | 2011 | — |
| −1 | K180820 | Tono Vue Non-Contact Tonometer | Crystalvue Medical Corporation | 2018 | — |
| 0 (this device) | K223739 | VS Tabletop Tonometer | Medimaging Integrated Solution, Inc. | 2023 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 2002 | 1 | 0 |
| 2019 | 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 HKX? 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 HKX device
- #1 K253039 Auto Kerato-Refracto Tonometer TRK-3 Omniascore 11.5 · 5 generations · no Class I recall
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K181260 | MiiS Horus Scope DPT 100Summary page 4…r and accessories Regulatory Class: Class II Product Code: HKX Predicate Device: Primary predicate device: K181260 Trade/Device Name: MiiS Horus Scope DPT 100 Regulation Number: 21 CFR 886.1930… | 2019 |
| * | K180820 | Tono Vue Non-Contact TonometerSummary page 4…and accessories Regulatory Class: Class II Product Code: HKX Secondary Predicate Device K180820 Trade/Device Name: Tono Vue Non-Contact Tonometer Regulation Number: 21 CFR 886.1930… | 2018 |
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 28 years and passes through 6 companies; a new generation was cleared every 5.7 years on median.
- None of the 8 ancestors has a recall.
How does its category compare?
All HKX devicesHKX Tonometer, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.
FDA decisions per year · HKX
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HKX
290in 2019
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HKX
No recall names HKX since 2007.
Adverse event reports per year · HKX
1in 2015
MAUDE reports naming product code HKX, 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 | 0 |
| 2008 | 2 | — | 0 | 1 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 1 | — | 0 | 1 |
| 2011 | 1 | — | 0 | 0 |
| 2012 | 1 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 1 | — | 0 | 1 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 1 | — | 0 | 0 |
| 2019 | 3 | 290 | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 1 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 1 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The VS Tabletop Tonometer is a digital tonometer intended to measure intraocular pressure of the human eye.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K223739 · printed Nov 5, 2026
Cite this page
510(k) Report. “K223739: VS Tabletop Tonometer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K223739
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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