510(k) Report

510(k) · Cleared

Cleared

Non-Contact Infrared Thermometer, model HL710H

K211744510(k) TraditionalCleared Nov 24, 2021170-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

Health & Life Co., Ltd. · FLL Continuous Measurement Thermometer

Cleared on Nov 24, 2021 as substantially equivalent to K191829 (Microlife Intellectual Property GmbH, 2020) after a 170-day review. Its family tree reaches back 5 generations to 2000.

Decided
Nov 24, 2021
Review
170 days
Class
Class II
Product code
FLL
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K000969 (2000). 9 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 5 generations backK000969 Microlife Digital Infrared Ear Thermometer, Model IR1DA1Microlife Corp. · 2000
  2. 4 generations backK020725 Microlife Digital Infrared Ear Thermometer, Model IR1DE1Microlife Corp. · 2002
  3. 3 generations backK033820 Microlife Digital Infrared Forehead Thermometer, Model FR1DM1Microlife Intellectual Property GmbH · 2004
  4. 2 generations backK100953 Microlife Non-Contact Infrared Forehead Thermometer, Model FR1DZ1Microlife Intellectual Property GmbH · 2010
  5. 1 generation backK191829 Microlife Non-Contact Infrared Forehead ThermometerMicrolife Intellectual Property GmbH · 2020
  6. This deviceK211744 Non-Contact Infrared Thermometer, model HL710HHealth & Life Co., Ltd. · 2021
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K000969Microlife Digital Infrared Ear Thermometer, Model IR1DA1Microlife Corp.2000—
−4K020725Microlife Digital Infrared Ear Thermometer, Model IR1DE1Microlife Corp.2002—
−3K033820Microlife Digital Infrared Forehead Thermometer, Model FR1DM1Microlife Intellectual Property GmbH2004—
−2K100953Microlife Non-Contact Infrared Forehead Thermometer, Model FR1DZ1Microlife Intellectual Property GmbH2010—
−1K191829Microlife Non-Contact Infrared Forehead ThermometerMicrolife Intellectual Property GmbH2020—
0 (this device)K211744Non-Contact Infrared Thermometer, model HL710HHealth & Life Co., Ltd.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010
200110
200410
200710
FIG. 1 — Lineage of K211744, 2000–2021Source: 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
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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
*K191829Microlife Non-Contact Infrared Forehead Thermometer
Summary page 6
…son: Product Specification Comparison Table of Subject Device HL710H, and Predicate Device Microlife Non-Contact Infrared Forehead Thermometer FR1DG1(NC200) (K191829) Comparison Subject Device Non- Predicate Device Results Items Contact Infrared…
Microlife Intellectual Property GmbH2020—
†K183663Microlife Digital Infrared Ear ThermometerMicrolife Intellectual Property GmbH2019—

Also cleared against K191829: 8 other devices →

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 21 years and passes through 3 companies; a new generation was cleared every 2.0 years on median.
  • None of the 9 ancestors has a recall.
  • 8 other devices also cite its predicate K191829.

How does its category compare?

All FLL devices

FLL Continuous Measurement Thermometer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, 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?

The Non-Contact Infrared Thermometer, model HL710H is intend for the measurement of human body temperature from the forehead. The device is indicated for use by people of all ages in the home.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K211744: Non-Contact Infrared Thermometer, model HL710H.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K211744

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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