510(k) Report

510(k) · Cleared

Cleared

Digital Radiography System (ManntiX B, ManntiX K)

K240841510(k) TraditionalCleared Dec 9, 2024257-day reviewClass II21 CFR 892.1720

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

Shenzhen Browiner Tech Co., Ltd. · IZL System, X-Ray, Mobile

Cleared on Dec 9, 2024 as substantially equivalent to K202353 (Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui), 2020) after a 257-day review. Its family tree reaches back 13 generations to 1990.

Decided
Dec 9, 2024
Review
257 days
Class
Class II
Product code
IZL
Recalls
None
Predicates
1

Its longest line of descent runs back 13 generations to K896095 (1990). 25 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 13 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
  2. 9 generations between
  3. 3 generations backK191451 CMDR 2CW (Multiple models)Minxray, Inc. · 2019
  4. 2 generations backK200726 AcuityPDRRadmedix, LLC · 2020
  5. 1 generation backK202353 SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging…Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui) · 2020
  6. This deviceK240841 Digital Radiography System (ManntiX B, ManntiX K)Shenzhen Browiner Tech Co., Ltd. · 2024
Show all 13 generations
  1. Root · 13 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
  2. 12 generations backK962699 Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V. · 1996
  3. 11 generations backK982862 Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V. · 1998
  4. 10 generations backK012211 Efilm WorkstationEfilm Medical, Inc. · 2001 · Recalled
  5. 9 generations backK020995 Efilm Workstation with ModulesEfilm Medical, Inc. · 2002 · Recalled
  6. 8 generations backK070618 Dicompacs, Model 5Oehm Und Rehbein GmbH · 2007
  7. 7 generations backK091364 Dicompacs, Model 5.2, Dicompacs DX-R, Model 1.4Oehm Und Rehbein GmbH · 2009
  8. 6 generations backK100449 Minxray Model CMDR-2SMinxray, Inc. · 2010
  9. 5 generations backK141885 CMDR-2ST & CMDR-2SLWT Digital Portable X-RayMinxray, Inc. · 2014
  10. 4 generations backK171353 CMDR 2ST (Multiple Models), CMDR 2SPE (Multiple Models), IntegrisMinxray, Inc. · 2017
  11. 3 generations backK191451 CMDR 2CW (Multiple models)Minxray, Inc. · 2019
  12. 2 generations backK200726 AcuityPDRRadmedix, LLC · 2020
  13. 1 generation backK202353 SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging…Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui) · 2020
  14. This deviceK240841 Digital Radiography System (ManntiX B, ManntiX K)Shenzhen Browiner Tech Co., Ltd. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K896095Images-on-Call Teleradiology SystemDevices & Services Co.1990—
−12K962699Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V.1996—
−11K982862Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V.1998—
−10K012211Efilm WorkstationEfilm Medical, Inc.20011
−9K020995Efilm Workstation with ModulesEfilm Medical, Inc.20022
−8K070618Dicompacs, Model 5Oehm Und Rehbein GmbH2007—
−7K091364Dicompacs, Model 5.2, Dicompacs DX-R, Model 1.4Oehm Und Rehbein GmbH2009—
−6K100449Minxray Model CMDR-2SMinxray, Inc.2010—
−5K141885CMDR-2ST & CMDR-2SLWT Digital Portable X-RayMinxray, Inc.2014—
−4K171353CMDR 2ST (Multiple Models), CMDR 2SPE (Multiple Models), IntegrisMinxray, Inc.2017—
−3K191451CMDR 2CW (Multiple models)Minxray, Inc.2019—
−2K200726AcuityPDRRadmedix, LLC2020—
−1K202353SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging SystemShantou Institute of Ultrasonic Instruments Co., Ltd. (Siui)2020—
0 (this device)K240841Digital Radiography System (ManntiX B, ManntiX K)Shenzhen Browiner Tech Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199810
199910
200110
200230
200310
200410
200510
200810
200910
FIG. 1 — Lineage of K240841, 1990–2024Source: 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 IZL? 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 IZL device

  1. #1 K242015 TOPAZ Mobile X-ray System (Models : TOPAZ-32D…score 19.9 · 19 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
*K202353SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging System
Summary page 6
…e Information Manufacturer Proprietary /Trade Name 510(K) Number Shantou Institute of SR-2300 Portable DR Imaging System K202353 Ultrasonic Instruments SR-2300S Portable DR Imaging System Co., Ltd. (SIUI) Device Name: SR-2300 Portable DR Imaging Sy…
Shantou Institute of Ultrasonic Instruments Co., Ltd. (Siui)2020—

Also cleared against K202353: 1 other device →

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 34 years and passes through 8 companies; a new generation was cleared every 2.6 years on median.
  • 3 of the 25 ancestors have a recall of any class.
  • 1 other device also cites its predicate K202353.

How does its category compare?

All IZL devices

IZL System, X-Ray, Mobile: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · IZL

11in 2025

2007: 32008: 42009: 32010: 32011: 62012: 32014: 72015: 42016: 62017: 72018: 82019: 92020: 92021: 132022: 162023: 32024: 92025: 112026 (partial year): 6
2007high 16 (2022) · low 0 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IZL

153in 2025

2007: 30 days median2008: 49 days median2009: 125 days median2010: 65 days median2011: 66 days median2012: 83 days median2014: 104 days median2015: 88 days median2016: 47 days median2017: 45 days median2018: 47 days median2019: 33 days median2020: 43 days median2021: 48 days median2022: 89 days median2023: 55 days median2024: 159 days median2025: 153 days median2026 (partial year): 157 days median
2007high 159 (2024) · low 30 (2007)2026

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

Recalls per year · IZL

47in 2025

2007: 72010: 42011: 62012: 52013: 102014: 42015: 42019: 22020: 12022: 12023: 62024: 52025: 472026 (partial year): 5
2007high 47 (2025) · low 0 (2008)2026

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

Adverse event reports per year · IZL

27in 2025

2007: 162008: 272009: 352010: 752011: 1182012: 242013: 172014: 512015: 302016: 332017: 352018: 272019: 402020: 482021: 472022: 322023: 772024: 392025: 27
2007high 118 (2011) · low 16 (2007)2025

MAUDE reports naming product code IZL, 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
2007330716
2008449027
20093125035
2010365475
20116666118
2012383524
20130—1017
20147104451
2015488430
2016647033
2017745035
2018847027
2019933240
2020943148
20211348047
20221689132
2023355677
20249159539
2025111534727
202661575—

What is it indicated for?

Intended for use by a qualified/trained physician or technician for the purpose of acquiring X-ray images of the desired parts of patient's anatomy (including head, cervical spine, chest, abdomen, lumbar spine, pelvis and extremities).

This device is not intended for mammography.

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. “K240841: Digital Radiography System (ManntiX B, ManntiX K).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K240841

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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