510(k) Report

510(k) · Cleared

Cleared

Ceragem Automatic Thermal Massager, Model CGM MB-1701 & CGM MB-1702

K220572510(k) TraditionalCleared Jun 17, 2022109-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

Ceragem Co., Ltd. · JFB Table, Physical Therapy, Multi Function

Cleared on Jun 17, 2022 as substantially equivalent to K202937 (Ceragem Co., Ltd., 2021) after a 109-day review. Its family tree reaches back 6 generations to 2000. 1 later device descends from it.

Decided
Jun 17, 2022
Review
109 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). 1 later device descends from it, 1 citing it directly.

  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 backK140592 Ceragem Automatic Thermal MassagerCeragem International, Inc. · 2014
  6. 1 generation backK202937 Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702Ceragem Co., Ltd. · 2021
  7. This deviceK220572 Ceragem Automatic Thermal Massager, Model CGM MB-1701 & CGM MB-1702Ceragem Co., Ltd. · 2022
  8. Descendant · cites it directly · 0 of its ownK240168 N7-SNuga Medical Co., Ltd. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K240168N7-SNuga Medical Co., Ltd. · 2024 · cites it directly0descendants
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—
−2K140592Ceragem Automatic Thermal MassagerCeragem International, Inc.2014—
−1K202937Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702Ceragem Co., Ltd.2021—
0 (this device)K220572Ceragem Automatic Thermal Massager, Model CGM MB-1701 & CGM MB-1702Ceragem Co., Ltd.2022—
+1K240168N7-SNuga Medical Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K220572, 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 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
Get a 510(k) Report

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
*K202937Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702
Summary page 4
…ss II • Product Code: JFB, IRP • 510(k) Identification Number: K220572 Primary Predicate Devices • Ceragem Automatic Thermal Massager Model CGM-MB-1701 & CGM-MB-1702, K202937 The predicate has not been subject to a design-related recall. Reference Device: • Air Compression Therapy Device, K193354 Pri…
Ceragem Co., Ltd.2021—
†K193354Air Compression Therapy DeviceShenzhen Dongjilian Electronics Co., Ltd.2020—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K240168N7-SNuga Medical Co., Ltd.20240

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 22 years and passes through 5 companies; a new generation was cleared every 3.0 years on median.
  • None of the 7 ancestors has a recall.
  • Of its descendants, K240168 (Nuga Medical Co., Ltd., 2024) has gone furthest, with 0 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. 2022, 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?

The intended use of the Ceragem Automatic Thermal Massager, Model CGM MB-1701 & CGM MB-1702 is to provide muscle relaxation therapy by delivering heat and soothing massage. Additionally, the product provides topical radiant infrared heat for: -Temporary relief of minor muscle and joint pain stiffness -Temporary relief of minor joint pain associated with arthritis -Temporary increase in local circulation where applied - Relaxation of muscles The Air Cell…

Read the full statement (110 words)

The intended use of the Ceragem Automatic Thermal Massager,

Model CGM MB-1701 & CGM MB-1702 is to provide muscle relaxation therapy by delivering heat and soothing massage. Additionally, the product provides topical radiant infrared heat for:

-Temporary relief of minor muscle and joint pain stiffness

-Temporary relief of minor joint pain associated with arthritis

-Temporary increase in local circulation where applied

- Relaxation of muscles

The Air Cell Massager (only CGM MB-1701) is indicated for the temporary relief of minor muscle aches and pains and for temporary increase in blood circulation to the treated areas. The Air Cell Massager stimulates kneading and stroking of tissues by using an inflatable garment.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K220572: Ceragem Automatic Thermal Massager, Model CGM MB-1701 & CGM MB-1702.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K220572

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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