510(k) Report

510(k) · Cleared

Cleared

Quest Intersegmental Roller Traction Table

K993461510(k) TraditionalCleared Jan 3, 200082-day reviewClass II21 CFR 890.5880

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

Icon Intl., LLC · JFB Table, Physical Therapy, Multi Function

Cleared on Jan 3, 2000 after an 82-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 14 later devices descend from it.

Decided
Jan 3, 2000
Review
82 days
Class
Class II
Product code
JFB
Recalls
None
Predicates
0

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

Descendants, by year cleared 2000: 1 descendant cleared2012: 2 descendants cleared2003: 1 descendant cleared2004: 1 descendant cleared2014: 1 descendant cleared2007: 1 descendant cleared2008: 1 descendant cleared2006: 1 descendant cleared2010: 1 descendant cleared2021: 2 descendants cleared2022: 1 descendant cleared2024: 1 descendant cleared200020052010201520202025
  1. This deviceK993461 Quest Intersegmental Roller Traction TableIcon Intl., LLC · 2000
  2. Descendant · cites it directly · 13 of its ownK002390 Quantum Intersegmental Traction Table 400, 401, 400H,401HLsi Intl., Inc. · 2000
  3. Descendant · 2 generations on · 11 of its ownK032449 Thermassage Energy Product, Model HY5000Migun Medical Instrument Co., Ltd. · 2003
  4. Descendant · 3 generations on · 10 of its ownK040031 Ceragem-C Thermal Acupressure MassagerCeragem Co., Ltd. · 2004
  5. Descendant · 4 generations on · 4 of its ownK140592 Ceragem Automatic Thermal MassagerCeragem International, Inc. · 2014
  6. Descendant · 4 generations on · 3 of its ownK062476 Ceragem RH1 Automatic Thermal MassagerCeragem International, Inc. · 2006

Showing 5 of 14 descendants. See all descendants

Descendants cleared per year

2000: 12003: 12004: 12006: 12007: 12008: 12010: 12012: 22014: 12021: 22022: 12024: 1
2000high 2 (2012) · low 0 (2001)2026

Most influential descendants

Showing 5 of 14 · See all
  • K002390Quantum Intersegmental Traction Table 400, 401, 400H,401HLsi Intl., Inc. · 2000 · cites it directly13descendants
  • K032449Thermassage Energy Product, Model HY5000Migun Medical Instrument Co., Ltd. · 2003 · 2 generations on11descendants
  • K040031Ceragem-C Thermal Acupressure MassagerCeragem Co., Ltd. · 2004 · 3 generations on10descendants
  • K140592Ceragem Automatic Thermal MassagerCeragem International, Inc. · 2014 · 4 generations on4descendants
  • K062476Ceragem RH1 Automatic Thermal MassagerCeragem International, Inc. · 2006 · 4 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K993461Quest Intersegmental Roller Traction TableIcon Intl., LLC2000—
+1K002390Quantum Intersegmental Traction Table 400, 401, 400H,401HLsi Intl., Inc.2000—
+2K032449Thermassage Energy Product, Model HY5000Migun Medical Instrument Co., Ltd.2003—
+3K040031Ceragem-C Thermal Acupressure MassagerCeragem Co., Ltd.2004—
+4K140592Ceragem Automatic Thermal MassagerCeragem International, Inc.2014—
+4K062476Ceragem RH1 Automatic Thermal MassagerCeragem International, Inc.2006—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200010
200310
200410
200610
200710
200810
201010
201220
201410
202120
202210
202410
FIG. 1 — Lineage of K993461, 2000–2024Source: 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 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JFB? 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 JFB device

  1. #1 K240168 N7-Sscore 9.8 · 7 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’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (14)

See all 14

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

NumberDeviceApplicantDecidedDescendants
K002390Quantum Intersegmental Traction Table 400, 401, 400H,401HLsi Intl., Inc.200013
K111588Legacy-500Mt Tables, LLC20120

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, K002390 (Lsi Intl., Inc., 2000) has gone furthest, with 13 descendants of its own.

How does its category compare?

All JFB devices

JFB Table, Physical Therapy, Multi Function: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JFB

3in 2025

2007: 12008: 12010: 22011: 22012: 22014: 12016: 12021: 22022: 12024: 22025: 3
2007high 3 (2025) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JFB

162in 2025

2025: 162 days median
2007high 162 (2025)2026

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

Recalls per year · JFB

No recall names JFB since 2007.

Adverse event reports per year · JFB

1in 2024

2007: 32008: 32009: 32010: 12011: 12012: 22013: 22020: 12022: 22024: 1
2007high 3 (2007) · low 0 (2014)2025

MAUDE reports naming product code JFB, 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
20071—03
20081—03
20090—03
20102—01
20112—01
20122—02
20130—02
20141—00
20150—00
20161—00
20170—00
20180—00
20190—00
20200—01
20212—00
20221—02
20230—00
20242—01
2025316200
20260—0—

What is it indicated for?

The Quest Intersegmental Roller Table uses a roller mechanism and electric

motors coupled with vibration and optional heat to release muscle tension and

deliver soothing massage by the movement of the roller carriage back and forth

from the cervical area to the lumbar area of the patient.

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K993461: Quest Intersegmental Roller Traction Table.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K993461

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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