510(k) Report

510(k) · Cleared

Cleared

Microlife Digital Infrared Ear Thermometer, Model Iridvi-1

K091040510(k) TraditionalCleared May 13, 200930-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

Microlife Intellectual Property GmbH · FLL Continuous Measurement Thermometer

Cleared on May 13, 2009 as substantially equivalent to K034023 (Microlife Intellectual Property GmbH, 2004) after a 30-day review. Its family tree reaches back 3 generations to 2000. 2 later devices descend from it.

Decided
May 13, 2009
Review
30 days
Class
Class II
Product code
FLL
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K000969 (2000). 4 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor2012: 1 descendant cleared2017: 1 descendant clearedK000969 · Microlife Digital Infrared Ear Thermometer, Model IR1DA1 · Microlife Corp. · 2000K020725 · Microlife Digital Infrared Ear Thermometer, Model IR1DE1 · Microlife Corp. · 2002K034023 · Microlife Digital Infrared Ear Thermometer, Model IR1DE1-1 · Microlife Intellectual Property GmbH · 2004200020052010201520202025
Other ancestors, by generationDescendants, by generation 3 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant K034023 · Microlife Digital Infrared Ear Thermometer, Model IR1DE1-1 · Microlife Intellectual Property GmbH · 2004K020725 · Microlife Digital Infrared Ear Thermometer, Model IR1DE1 · Microlife Corp. · 2002K000969 · Microlife Digital Infrared Ear Thermometer, Model IR1DA1 · Microlife Corp. · 20000
  1. Root · 3 generations backK000969 Microlife Digital Infrared Ear Thermometer, Model IR1DA1Microlife Corp. · 2000
  2. 2 generations backK020725 Microlife Digital Infrared Ear Thermometer, Model IR1DE1Microlife Corp. · 2002
  3. 1 generation backK034023 Microlife Digital Infrared Ear Thermometer, Model IR1DE1-1Microlife Intellectual Property GmbH · 2004
  4. This deviceK091040 Microlife Digital Infrared Ear Thermometer, Model Iridvi-1Microlife Intellectual Property GmbH · 2009
  5. Descendant · cites it directly · 1 of its ownK113141 Microlife Dual Mode Thermometer,Model IFR1MJ1Microlife Intellectual Property GmbH · 2012
  6. Descendant · 2 generations on · 0 of its ownK163256 Dual Mode Infrared ThermometerIntelliworks, LLC · 2017

Most influential descendants

Showing 2 of 2 · See all
  • K113141Microlife Dual Mode Thermometer,Model IFR1MJ1Microlife Intellectual Property GmbH · 2012 · cites it directly1descendant
  • K163256Dual Mode Infrared ThermometerIntelliworks, LLC · 2017 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K000969Microlife Digital Infrared Ear Thermometer, Model IR1DA1Microlife Corp.2000—
−2K020725Microlife Digital Infrared Ear Thermometer, Model IR1DE1Microlife Corp.2002—
−1K034023Microlife Digital Infrared Ear Thermometer, Model IR1DE1-1Microlife Intellectual Property GmbH2004—
0 (this device)K091040Microlife Digital Infrared Ear Thermometer, Model Iridvi-1Microlife Intellectual Property GmbH2009—
+1K113141Microlife Dual Mode Thermometer,Model IFR1MJ1Microlife Intellectual Property GmbH2012—
+2K163256Dual Mode Infrared ThermometerIntelliworks, LLC2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201710
FIG. 1 — Lineage of K091040, 2000–2017Source: 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
*K034023Microlife Digital Infrared Ear Thermometer, Model IR1DE1-1
Summary page 1
…Microlife Digital Infrared Ear Thermometer, Model IR1 DV1 -1 3. Predicate Device Information: Microlife Digital Infrared Ear Thermometer, Model IRIDEI-11, K#034023 4. Device Description: The Microlife Digital Infrared Ear Thermometer, Model IR1DV1I- isan electronic thermo…
Microlife Intellectual Property GmbH2004—

Also cleared against K034023: 2 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K113141Microlife Dual Mode Thermometer,Model IFR1MJ1Microlife Intellectual Property GmbH20121

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 9 years and passes through 2 companies; a new generation was cleared every 1.8 years on median.
  • None of the 4 ancestors has a recall.
  • Of its descendants, K113141 (Microlife Intellectual Property GmbH, 2012) has gone furthest, with 1 descendant of its own.
  • 2 other devices also cite its predicate K034023.

How does its category compare?

All FLL devices

FLL Continuous Measurement Thermometer: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, 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 Microlife Digital Infrared Ear Thermometer IR1DVI-1 is an electronic clinical thermometer

using an infrared sensor to detect body temperature from the auditory canal in the neonatal,

pediatric and adult population used in the home setting.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K091040: Microlife Digital Infrared Ear Thermometer, Model Iridvi-1.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K091040

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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