510(k) Report

510(k) · Cleared

Cleared

Nexus IR30 Non-Contact Infrared Forehead Thermometer

K122221510(k) SpecialCleared Mar 29, 2013247-day reviewClass II21 CFR 880.2910

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

Taidoc Technology Corporation · FLL Continuous Measurement Thermometer

Cleared on Mar 29, 2013 as substantially equivalent to K113159 (Taidoc Technology Corporation, 2012) after a 247-day review. Its family tree reaches back 3 generations to 2006. 2 later devices descend from it.

Decided
Mar 29, 2013
Review
247 days
Class
Class II
Product code
FLL
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K061800 (2006). 2 later devices descend from it, 2 citing it directly.

  1. Root · 3 generations backK061800 Clever TD-1112 Ear/Skin/Surface IR ThermometerTaidoc Technology Corporation · 2006
  2. 2 generations backK081445 Fora Comfortscan Ear Thermometer, Models TD-1261A; TD-1261BTaidoc Technology Corporation · 2008
  3. 1 generation backK113159 U-Right TD-1240 ThermometerTaidoc Technology Corporation · 2012
  4. This deviceK122221 Nexus IR30 Non-Contact Infrared Forehead ThermometerTaidoc Technology Corporation · 2013
  5. Descendant · cites it directly · 0 of its ownK160802 Infrared Forehead Thermometer, FT-100AHangzhou Universal Electronic Co., Ltd. · 2016
  6. Descendant · cites it directly · 0 of its ownK133113 Kingtech Forehead ThermometerKingtech Enterprise, Ltd. · 2013

Most influential descendants

Showing 2 of 2 · See all
  • K160802Infrared Forehead Thermometer, FT-100AHangzhou Universal Electronic Co., Ltd. · 2016 · cites it directly0descendants
  • K133113Kingtech Forehead ThermometerKingtech Enterprise, Ltd. · 2013 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K061800Clever TD-1112 Ear/Skin/Surface IR ThermometerTaidoc Technology Corporation2006—
−2K081445Fora Comfortscan Ear Thermometer, Models TD-1261A; TD-1261BTaidoc Technology Corporation2008—
−1K113159U-Right TD-1240 ThermometerTaidoc Technology Corporation2012—
0 (this device)K122221Nexus IR30 Non-Contact Infrared Forehead ThermometerTaidoc Technology Corporation2013—
+1K160802Infrared Forehead Thermometer, FT-100AHangzhou Universal Electronic Co., Ltd.2016—
+1K133113Kingtech Forehead ThermometerKingtech Enterprise, Ltd.2013—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201310
201610
FIG. 1 — Lineage of K122221, 2006–2016Source: 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 FLL? 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 FLL device

  1. #1 K191829 Microlife Non-Contact Infrared Forehead…score 26.7 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) 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.

TypeNumberDeviceApplicantDecidedRecalls
*K113159U-Right TD-1240 Thermometer
Summary page 2
…mber: kI 13159 C. Comparison with predicate: The Nexus 1R130 Thermometer is substantially equivalent to the predicate device U-RIGHT TD- 1240 Thermometer (k113159) made by TaiDoc Technology Corporation, for the following reasons: I) It has the same Indications for use as the predic…
Taidoc Technology Corporation2012—

Also cleared against K113159: 2 other devices →

What descends from it? (2)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K160802Infrared Forehead Thermometer, FT-100AHangzhou Universal Electronic Co., Ltd.20160
K133113Kingtech Forehead ThermometerKingtech Enterprise, Ltd.20130

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 7 years and passes through 1 company; a new generation was cleared every 2.1 years on median.
  • None of the 3 ancestors has a recall.
  • Of its descendants, K160802 (Hangzhou Universal Electronic Co., Ltd., 2016) has gone furthest, with 0 descendants of its own.
  • 2 other devices also cite its predicate K113159.

How does its category compare?

All FLL devices

FLL Continuous Measurement Thermometer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.

FDA decisions per year · FLL

6in 2025

2007: 152008: 142009: 132010: 242011: 202012: 172013: 142014: 72015: 32016: 222017: 162018: 352019: 222020: 212021: 432022: 242023: 172024: 132025: 62026 (partial year): 2
2007high 43 (2021) · low 3 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FLL

131in 2025

2007: 81 days median2008: 59 days median2009: 84 days median2010: 88 days median2011: 113 days median2012: 126 days median2013: 149 days median2014: 199 days median2015: 270 days median2016: 157 days median2017: 174 days median2018: 209 days median2019: 198 days median2020: 194 days median2021: 218 days median2022: 218 days median2023: 295 days median2024: 223 days median2025: 131 days median
2007high 295 (2023) · low 59 (2008)2026

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

Recalls per year · FLL

1in 2025

2011: 12015: 12017: 22018: 12019: 52025: 12026 (partial year): 1
2007high 5 (2019) · low 0 (2007)2026

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

Adverse event reports per year · FLL

73in 2025

2007: 42008: 132009: 92010: 92011: 182012: 262013: 162014: 542015: 532016: 582017: 1182018: 512019: 522020: 532021: 1152022: 1422023: 1012024: 1182025: 73
2007high 142 (2022) · low 4 (2007)2025

MAUDE reports naming product code FLL, 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
2007158104
20081459013
2009138409
2010248809
201120113118
201217126026
201314149016
20147199054
20153270153
201622157058
2017161742118
201835209151
201922198552
202021194053
2021432180115
2022242180142
2023172950101
2024132230118
20256131173
20262—1—

What is it indicated for?

Nexus IR30 Thermometer is an electronic thermometer using an infrared sensor to detect human body temperature from the surface of human skin without contact. It is for use on people of all ages (infants, children, adolescents, and adults) in the homecare environment.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K122221: Nexus IR30 Non-Contact Infrared Forehead Thermometer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122221

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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