510(k) Report

510(k) · Cleared

Cleared

Non-Contact Tear Film Thermogragh

K111771510(k) TraditionalCleared Nov 30, 2011160-day reviewClass II21 CFR 886.1120

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

United Integrated Services Co., Ltd. · HKI Camera, Ophthalmic, Ac-Powered

Cleared on Nov 30, 2011 as substantially equivalent to K091935 (Tearscience, Inc., 2009) after a 160-day review. Its family tree reaches back 4 generations to 1991. 1 later device descends from it.

Decided
Nov 30, 2011
Review
160 days
Class
Class II
Product code
HKI
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K913929 (1991). 6 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 4 generations backK913929 DFC-1024 & DFC-512 Digital Imaging SystemOphthalmic Imaging Systems · 1991 · Recalled
  2. 3 generations backK971685 Imagescape Digital Retinal Image SystemTomey Corporation USA · 1997
  3. 2 generations backK980295 Ophthavision Imaging SystemMrp Group, Inc. · 1998
  4. 1 generation backK091935 Lipiview Ocular Surface InterferometerTearscience, Inc. · 2009
  5. This deviceK111771 Non-Contact Tear Film ThermograghUnited Integrated Services Co., Ltd. · 2011
  6. Descendant · cites it directly · 0 of its ownK253176 TearViewBeyond 700 Pty, Ltd. · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K253176TearViewBeyond 700 Pty, Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K913929DFC-1024 & DFC-512 Digital Imaging SystemOphthalmic Imaging Systems19915
−3K971685Imagescape Digital Retinal Image SystemTomey Corporation USA1997—
−2K980295Ophthavision Imaging SystemMrp Group, Inc.1998—
−1K091935Lipiview Ocular Surface InterferometerTearscience, Inc.2009—
0 (this device)K111771Non-Contact Tear Film ThermograghUnited Integrated Services Co., Ltd.2011—
+1K253176TearViewBeyond 700 Pty, Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K111771, 1991–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K253176 TearViewscore 12.7 · 5 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K091935Lipiview Ocular Surface Interferometer
Summary page 1
…y and Effectiveness Information * Predicate Device: Claim of Substantial Equivalence (SE) is made to LipView Ocular Surface Interferometer (K(091935) * Device Description: The ocular surface temperature is measured by the thermal sensor of the thermograph syst…
Tearscience, Inc.2009—

Also cleared against K091935: 3 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K253176TearViewBeyond 700 Pty, Ltd.20260

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 20 years and passes through 5 companies; a new generation was cleared every 5.6 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K253176 (Beyond 700 Pty, Ltd., 2026) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K091935.

How does its category compare?

All HKI devices

HKI Camera, Ophthalmic, Ac-Powered: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · HKI

4in 2025

2007: 22008: 52009: 112010: 62011: 72012: 52013: 72014: 42016: 42017: 22018: 62019: 42020: 52021: 42022: 12023: 52024: 32025: 42026 (partial year): 2
2007high 11 (2009) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HKI

167in 2025

2008: 29 days median2009: 104 days median2010: 140 days median2011: 160 days median2012: 179 days median2013: 141 days median2014: 135 days median2016: 146 days median2018: 71 days median2019: 73 days median2020: 182 days median2021: 155 days median2023: 259 days median2024: 28 days median2025: 167 days median
2007high 259 (2023) · low 28 (2024)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HKI

1in 2018

2012: 12016: 12017: 12018: 1
2007high 1 (2012) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · HKI

1in 2023

2007: 32008: 12009: 12012: 22013: 222014: 32015: 32016: 662017: 202018: 142020: 52021: 32022: 12023: 1
2007high 66 (2016) · low 0 (2010)2025

MAUDE reports naming product code HKI, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—03
200852901
20091110401
2010614000
2011716000
2012517912
20137141022
2014413503
20150—03
20164146166
20172—120
2018671114
201947300
2020518205
2021415503
20221—01
2023525901
202432800
2025416700
20262—0—

What is it indicated for?

The UIS Non-Contact Thermograph System is an ophthalmic imaging device that stores,

archives, and manipulates digital images of ocular surface temperature measurements taken

by a physician in adult patients.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K111771: Non-Contact Tear Film Thermogragh.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111771

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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