510(k) Report

510(k) · Cleared

Cleared

Thermal Massage Bed, Model 2D-GX

K102281510(k) SpecialCleared Dec 22, 2010133-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

Inarex Corporation · JFB Table, Physical Therapy, Multi Function

Cleared on Dec 22, 2010 as substantially equivalent to K080554 (Inarex Corporation, 2008) after a 133-day review. Its family tree reaches back 6 generations to 2000.

Decided
Dec 22, 2010
Review
133 days
Class
Class II
Product code
JFB
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K993461 (2000). 7 ancestors in all, the oldest K933443 (1994). No later device cites it as a predicate yet.

  1. Root · 6 generations backK993461 Quest Intersegmental Roller Traction TableIcon Intl., LLC · 2000
  2. 5 generations backK002390 Quantum Intersegmental Traction Table 400, 401, 400H,401HLsi Intl., Inc. · 2000
  3. 4 generations backK032449 Thermassage Energy Product, Model HY5000Migun Medical Instrument Co., Ltd. · 2003
  4. 3 generations backK040031 Ceragem-C Thermal Acupressure MassagerCeragem Co., Ltd. · 2004
  5. 2 generations backK062476 Ceragem RH1 Automatic Thermal MassagerCeragem International, Inc. · 2006
  6. 1 generation backK080554 Inarex, Model 2D-LXInarex Corporation · 2008
  7. This deviceK102281 Thermal Massage Bed, Model 2D-GXInarex Corporation · 2010
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K993461Quest Intersegmental Roller Traction TableIcon Intl., LLC2000—
−5K002390Quantum Intersegmental Traction Table 400, 401, 400H,401HLsi Intl., Inc.2000—
−4K032449Thermassage Energy Product, Model HY5000Migun Medical Instrument Co., Ltd.2003—
−3K040031Ceragem-C Thermal Acupressure MassagerCeragem Co., Ltd.2004—
−2K062476Ceragem RH1 Automatic Thermal MassagerCeragem International, Inc.2006—
−1K080554Inarex, Model 2D-LXInarex Corporation2008—
0 (this device)K102281Thermal Massage Bed, Model 2D-GXInarex Corporation2010—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
FIG. 1 — Lineage of K102281, 2000–2010Source: 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 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
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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
*K080554Inarex, Model 2D-LX
Summary page 1
…al Name: Thermal massage bed 3. Proprietary Name: Thermal massage bed (2D-LX) 4. Classification /Product Code: Class 11 / JEB (21 CER 890.5880) 5. 5 10(K) Number: K080554 F. Intended Use Thernnal Massage fled (2D-GX) is a device intended to provide patients with muscle relaxation therapy by…
Inarex Corporation2008—

What descends from it?

No later submission names this one as a predicate yet.

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 10 years and passes through 6 companies; a new generation was cleared every 2.3 years on median.
  • None of the 7 ancestors has a recall.

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. 2010, this device’s year, is highlighted.

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?

Thermal Massage Bed (2D-GX) is a device intended to provide patients with muscle relaxation therapy by delivering heat and soothing massage.

Additionally, the infrared lamps provide topical heating for:

-Temporary relief of minor muscle and joint pain, and stiffness

-Temporary relief of minor joint pain associated with arthritis

-Temporary increase in local circulation where applied

-Relaxation of muscles

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K102281: Thermal Massage Bed, Model 2D-GX.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K102281

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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