510(k) Report

510(k) · Cleared

Cleared

U-Right TD-3132 Blood Pressure Monitor, Fora P 20 Blood Pressure Monitor, Model TD-3132, TD-3132

K092106510(k) TraditionalCleared Jan 25, 2010195-day reviewClass II21 CFR 870.1130

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

Taidoc Technology Corporation · DXN System, Measurement, Blood-Pressure, Non-Invasive

Cleared on Jan 25, 2010 as substantially equivalent to K082734 (A&D Engineering, Inc., 2008) after a 195-day review. Its family tree reaches back 4 generations to 1998. 10 later devices descend from it.

Decided
Jan 25, 2010
Review
195 days
Class
Class II
Product code
DXN
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K982481 (1998). 6 ancestors in all. 10 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2002: 1 other ancestor2010: 2 descendants cleared2011: 3 descendants cleared2014: 2 descendants cleared2018: 1 descendant cleared2012: 1 descendant cleared2019: 1 descendant clearedK982481 · A&D Medical UA-767PC Digital Blood Pressure Monitor · A&D Engineering, Inc. · 1998K040371 · A & D Medical UA-767BT Digital Blood Pressure Monitor · A&D Engineering, Inc. · 2004K043217 · A&D Medical UA-767PBT Digital Blood Pressure Monitor · A&D Engineering, Inc. · 2005 · recalledK082734 · A&D Medical UA-851THW Digital Blood Pressure Monitor · A&D Engineering, Inc. · 20081995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor3 generations back: 1 other ancestor 1 generation forward: 5 descendants2 generations forward: 4 descendants3 generations forward: 1 descendant K082734 · A&D Medical UA-851THW Digital Blood Pressure Monitor · A&D Engineering, Inc. · 2008K043217 · A&D Medical UA-767PBT Digital Blood Pressure Monitor · A&D Engineering, Inc. · 2005 · recalledK040371 · A & D Medical UA-767BT Digital Blood Pressure Monitor · A&D Engineering, Inc. · 2004K982481 · A&D Medical UA-767PC Digital Blood Pressure Monitor · A&D Engineering, Inc. · 19980
  1. Root · 4 generations backK982481 A&D Medical UA-767PC Digital Blood Pressure MonitorA&D Engineering, Inc. · 1998
  2. 3 generations backK040371 A & D Medical UA-767BT Digital Blood Pressure MonitorA&D Engineering, Inc. · 2004
  3. 2 generations backK043217 A&D Medical UA-767PBT Digital Blood Pressure MonitorA&D Engineering, Inc. · 2005 · Recalled
  4. 1 generation backK082734 A&D Medical UA-851THW Digital Blood Pressure MonitorA&D Engineering, Inc. · 2008
  5. This deviceK092106 U-Right TD-3132 Blood Pressure Monitor, Fora P 20 Blood Pressure…Taidoc Technology Corporation · 2010
  6. Descendant · cites it directly · 2 of its ownK112216 U-Right TD-3128 Blood Pressure Monitoring SystemTaidoc Technology Corporation · 2011
  7. Descendant · 2 generations on · 1 of its ownK133588 Fora Care Blood Pressure Monitoring SystemForacare, Inc. · 2014
  8. Descendant · cites it directly · 1 of its ownK112274 U-Right TD-3135 Blood Pressure Monitoring SystemTaidoc Technology Corporation · 2011
  9. Descendant · cites it directly · 1 of its ownK100658 U-Right TD-3127 Blood Pressure Monitoring SystemTaidoc Technology Corporation · 2010
  10. Descendant · cites it directly · 1 of its ownK101259 V-Trust TD-8002 Multi-Parameter Spot-Check Monitor Model TD-8002Taidoc Technology Corporation · 2010

Showing 5 of 10 descendants. See all descendants

Descendants cleared per year

2010: 22011: 32012: 12014: 22018: 12019: 1
2010high 3 (2011) · low 0 (2013)2026

Most influential descendants

Showing 5 of 10 · See all
  • K112216U-Right TD-3128 Blood Pressure Monitoring SystemTaidoc Technology Corporation · 2011 · cites it directly2descendants
  • K133588Fora Care Blood Pressure Monitoring SystemForacare, Inc. · 2014 · 2 generations on1descendant
  • K112274U-Right TD-3135 Blood Pressure Monitoring SystemTaidoc Technology Corporation · 2011 · cites it directly1descendant
  • K100658U-Right TD-3127 Blood Pressure Monitoring SystemTaidoc Technology Corporation · 2010 · cites it directly1descendant
  • K101259V-Trust TD-8002 Multi-Parameter Spot-Check Monitor Model TD-8002Taidoc Technology Corporation · 2010 · cites it directly1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K982481A&D Medical UA-767PC Digital Blood Pressure MonitorA&D Engineering, Inc.1998—
−3K040371A & D Medical UA-767BT Digital Blood Pressure MonitorA&D Engineering, Inc.2004—
−2K043217A&D Medical UA-767PBT Digital Blood Pressure MonitorA&D Engineering, Inc.20051
−1K082734A&D Medical UA-851THW Digital Blood Pressure MonitorA&D Engineering, Inc.2008—
0 (this device)K092106U-Right TD-3132 Blood Pressure Monitor, Fora P 20 Blood Pressure Monitor…Taidoc Technology Corporation2010—
+1K112216U-Right TD-3128 Blood Pressure Monitoring SystemTaidoc Technology Corporation2011—
+2K133588Fora Care Blood Pressure Monitoring SystemForacare, Inc.2014—
+1K112274U-Right TD-3135 Blood Pressure Monitoring SystemTaidoc Technology Corporation2011—
+1K100658U-Right TD-3127 Blood Pressure Monitoring SystemTaidoc Technology Corporation2010—
+1K101259V-Trust TD-8002 Multi-Parameter Spot-Check Monitor Model TD-8002Taidoc Technology Corporation2010—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200210
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201020
201130
201210
201420
201810
201910
FIG. 1 — Lineage of K092106, 1998–2019Source: 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 DXN? 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 DXN device

  1. #1 K222125 Arm Blood Pressure Monitor, models AOJ-30A…score 18.5 · 8 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
*K082734A&D Medical UA-851THW Digital Blood Pressure Monitor
Summary page 1
…de/Proprietary Name:A&D Medical UA-85 1 THW Digital Blood Pressure Monitor Common/Usual Name: blood pressure monitor Manufacturer: A&D Engineering, Inc. 5 10 (k) Number: K082734 4. Device Description The TD-3 132 is an arm type blood pressure monitor. The device includes setting button, function button, L…
A&D Engineering, Inc.2008—

Also cleared against K082734: 1 other device →

What descends from it? (10)

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

NumberDeviceApplicantDecidedDescendants
K112216U-Right TD-3128 Blood Pressure Monitoring SystemTaidoc Technology Corporation20112
K112274U-Right TD-3135 Blood Pressure Monitoring SystemTaidoc Technology Corporation20111
K100658U-Right TD-3127 Blood Pressure Monitoring SystemTaidoc Technology Corporation20101
K101259V-Trust TD-8002 Multi-Parameter Spot-Check Monitor Model TD-8002Taidoc Technology Corporation20101
K110044Fora P30 Plus Multi-Mode Blood Pressure Monitoring SystemForacare, Inc.20110

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 12 years and passes through 2 companies; a new generation was cleared every 3.7 years on median.
  • 1 of the 6 ancestors has a recall of any class.
  • Of its descendants, K112216 (Taidoc Technology Corporation, 2011) has gone furthest, with 2 descendants of its own.
  • 1 other device also cites its predicate K082734.

How does its category compare?

All DXN devices

DXN System, Measurement, Blood-Pressure, Non-Invasive: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · DXN

28in 2025

2007: 272008: 232009: 462010: 432011: 342012: 362013: 342014: 292015: 302016: 302017: 332018: 222019: 332020: 242021: 232022: 252023: 352024: 172025: 282026 (partial year): 29
2007high 46 (2009) · low 17 (2024)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DXN

142in 2025

2007: 118 days median2008: 82 days median2009: 73 days median2010: 94 days median2011: 72 days median2012: 116 days median2013: 150 days median2014: 133 days median2015: 97 days median2016: 144 days median2017: 184 days median2018: 235 days median2019: 156 days median2020: 198 days median2021: 190 days median2022: 137 days median2023: 182 days median2024: 107 days median2025: 142 days median2026 (partial year): 147 days median
2007high 235 (2018) · low 72 (2011)2026

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

Recalls per year · DXN

3in 2024

2008: 12009: 32011: 12013: 12016: 12019: 12024: 3
2007high 3 (2009) · low 0 (2007)2026

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

Adverse event reports per year · DXN

239in 2025

2007: 212008: 82009: 172010: 142011: 102012: 192013: 722014: 472015: 622016: 542017: 902018: 6172019: 962020: 1302021: 1622022: 1552023: 1622024: 2702025: 239
2007high 617 (2018) · low 8 (2008)2025

MAUDE reports naming product code DXN, 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
200727118021
2008238218
20094673317
20104394014
20113472110
201236116019
201334150172
201429133047
20153097062
201630144154
201733184090
2018222350617
201933156196
2020241980130
2021231900162
2022251370155
2023351820162
2024171073270
2025281420239
2026291470—

What is it indicated for?

The FORA P20 Blood Pressure Monitor /U-RIGHT TD-3 132 Blood Pressure Monitor is intended to be used to measure non-invasively the systolic and diastolic blood pressure and pulse rate by using a non-invasive technique in which an inflatable cuff is wrapped on the upper arm. This system should only be used for the testing on people over 18 years of age and over.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K092106: U-Right TD-3132 Blood Pressure Monitor, Fora P 20 Blood Pressure Monitor, Model TD-3132, TD-3132.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K092106

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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