510(k) Report

510(k) · Cleared

Recalled · Class II · 2012

Exac-Temp & Clini-Temp Probe W/Temperature Sensor

K925791510(k) TraditionalCleared Feb 25, 1994466-day reviewClass II21 CFR 880.2910Recalls 1

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

Deroyal Industries, Inc. · FLL Continuous Measurement Thermometer

Cleared on Feb 25, 1994 after a 466-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 10 later devices descend from it. It has been recalled once.

Decided
Feb 25, 1994
Review
466 days
Class
Class II
Product code
FLL
Recalls
1
Predicates
0

10 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2005: 1 descendant cleared2020: 3 descendants cleared2013: 1 descendant cleared2022: 1 descendant cleared2026: 1 descendant cleared2018: 2 descendants cleared2023: 1 descendant cleared1990200020102020
  1. This deviceK925791 Exac-Temp & Clini-Temp Probe W/Temperature SensorDeroyal Industries, Inc. · 1994
  2. Descendant · cites it directly · 6 of its ownK051873 Disposable Temperature, Skin and Esophageal ProbesGE Healthcare · 2005 · Recalled
  3. Descendant · 2 generations on · 5 of its ownK121999 General Purpose Temperature Probe, Skin Temperature ProbeDraeger Medical GmbH · 2013
  4. Descendant · cites it directly · 2 of its ownK200631 DeRoyal Temperature Monitoring ProbeDeroyal Industries, Inc. · 2020
  5. Descendant · 3 generations on · 2 of its ownK181967 Disposable Temperature ProbeShenzhen Launch Electrical Co., Ltd. · 2018
  6. Descendant · 4 generations on · 1 of its ownK193338 Med-link Reusable Temperature Probes, Med-link Disposable…Shenzhen Med-Link Electronics Tech Co., Ltd. · 2020

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2005: 12013: 12018: 22020: 32022: 12023: 12026: 1
2005high 3 (2020) · low 0 (2006)2026

Most influential descendants

Showing 5 of 10 · See all
  • K051873Disposable Temperature, Skin and Esophageal ProbesGE Healthcare · 2005 · cites it directly6descendants
  • K121999General Purpose Temperature Probe, Skin Temperature ProbeDraeger Medical GmbH · 2013 · 2 generations on5descendants
  • K200631DeRoyal Temperature Monitoring ProbeDeroyal Industries, Inc. · 2020 · cites it directly2descendants
  • K181967Disposable Temperature ProbeShenzhen Launch Electrical Co., Ltd. · 2018 · 3 generations on2descendants
  • K193338Med-link Reusable Temperature Probes, Med-link Disposable Temperature ProbesShenzhen Med-Link Electronics Tech Co., Ltd. · 2020 · 4 generations on1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K925791Exac-Temp & Clini-Temp Probe W/Temperature SensorDeroyal Industries, Inc.1994—
+1K051873Disposable Temperature, Skin and Esophageal ProbesGE Healthcare20051
+2K121999General Purpose Temperature Probe, Skin Temperature ProbeDraeger Medical GmbH2013—
+1K200631DeRoyal Temperature Monitoring ProbeDeroyal Industries, Inc.2020—
+3K181967Disposable Temperature ProbeShenzhen Launch Electrical Co., Ltd.2018—
+4K193338Med-link Reusable Temperature Probes, Med-link Disposable Temperature ProbesShenzhen Med-Link Electronics Tech Co., Ltd.2020—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200510
201310
201820
202030
202210
202310
202610
FIG. 1 — Lineage of K925791, 1994–2026Source: 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), 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (10)

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

NumberDeviceApplicantDecidedDescendants
K051873Disposable Temperature, Skin and Esophageal ProbesGE Healthcare20056
K200631DeRoyal Temperature Monitoring ProbeDeroyal Industries, Inc.20202

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Aug 17, 2012Class IIZ-0407-2013Device DesignThere is a potential for epistaxis during use of the Disposable General Purpose 9 French Temperature Probe.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K051873 (GE Healthcare, 2005) has gone furthest, with 6 descendants of its own.

How does its category compare?

All FLL devices

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

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—
Cite this page

510(k) Report. “K925791: Exac-Temp & Clini-Temp Probe W/Temperature Sensor.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K925791

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026