510(k) Report

510(k) · Cleared

Cleared

Orgentec Anti-Tpo Elisa

K952129510(k) TraditionalCleared Jun 20, 199543-day reviewClass II21 CFR 866.5870

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

American Laboratory Products Co., Ltd. · JZO System, Test, Thyroid Autoantibody

Cleared on Jun 20, 1995 after a 43-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it.

Decided
Jun 20, 1995
Review
43 days
Class
Class II
Product code
JZO
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1999: 1 descendant cleared1995200020052010201520202025
  1. This deviceK952129 Orgentec Anti-Tpo ElisaAmerican Laboratory Products Co., Ltd. · 1995
  2. Descendant · cites it directly · 0 of its ownK992791 Brahms Diagnostica Dynotest Anti-TpoBrahms Diagnostica, LLC · 1999

Most influential descendants

Showing 1 of 1 · See all
  • K992791Brahms Diagnostica Dynotest Anti-TpoBrahms Diagnostica, LLC · 1999 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K952129Orgentec Anti-Tpo ElisaAmerican Laboratory Products Co., Ltd.1995—
+1K992791Brahms Diagnostica Dynotest Anti-TpoBrahms Diagnostica, LLC1999—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199910
FIG. 1 — Lineage of K952129, 1995–1999Source: 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 JZO? 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 JZO device

  1. #1 K250250 ADVIA Centaur Anti-Thyroid Peroxidase IIscore 10.5 · 2 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?

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

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K992791Brahms Diagnostica Dynotest Anti-TpoBrahms Diagnostica, LLC19990

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?

  • Of its descendants, K992791 (Brahms Diagnostica, LLC, 1999) has gone furthest, with 0 descendants of its own.

How does its category compare?

All JZO devices

JZO System, Test, Thyroid Autoantibody: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JZO

1in 2025

2008: 22009: 22010: 12016: 22020: 12023: 22024: 12025: 1
2007high 2 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JZO

Too few JZO 510(k)s in any year since 2007 to give a median.

Recalls per year · JZO

1in 2025

2025: 1
2007high 1 (2025) · low 0 (2007)2026

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

Adverse event reports per year · JZO

44in 2025

2010: 12011: 52012: 42013: 42014: 22015: 42016: 82017: 122018: 352019: 392020: 172021: 192022: 252023: 332024: 292025: 44
2007high 44 (2025) · low 0 (2007)2025

MAUDE reports naming product code JZO, 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
20070—00
20082—00
20092—00
20101—01
20110—05
20120—04
20130—04
20140—02
20150—04
20162—08
20170—012
20180—035
20190—039
20201—017
20210—019
20220—025
20232—033
20241—029
20251—144
20260—0—
Cite this page

510(k) Report. “K952129: Orgentec Anti-Tpo Elisa.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K952129

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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