510(k) Report

510(k) · Cleared

Cleared

Efai Pacs Picture Archiving and Communication System Pro

K232100510(k) SpecialCleared Aug 8, 202325-day reviewClass II21 CFR 892.2050

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

Ever Fortune.Ai, Co., Ltd. · LLZ System, Image Processing, Radiological

Cleared on Aug 8, 2023 as substantially equivalent to K211257 (Ever Fortune.Ai, Co., Ltd., 2021) after a 25-day review. Its family tree reaches back 6 generations to 1993.

Decided
Aug 8, 2023
Review
25 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K922164 (1993). 10 ancestors in all, the oldest K920319 (1992). No later device cites it as a predicate yet.

  1. Root · 6 generations backK922164 Raytel Digital Imaging SystemsOlicon Imaging Systems, Inc. · 1993
  2. 5 generations backK973959 Olicon Imaging Systems, Inc. 02-Workstation and/or Pacsview SoftwareOlicon Imaging Systems, Inc. · 1997
  3. 4 generations backK043146 Horizon Medical ImagingMckesson Medical Imaging Company · 2005 · Recalled
  4. 3 generations backK152186 HealthMyne PACSHealthmyne, Inc. · 2015
  5. 2 generations backK171544 Arterys ViewerArterys, Inc. · 2017
  6. 1 generation backK211257 EFAI PACS Picture Archiving and Communication SystemEver Fortune.Ai, Co., Ltd. · 2021
  7. This deviceK232100 Efai Pacs Picture Archiving and Communication System ProEver Fortune.Ai, Co., Ltd. · 2023
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K922164Raytel Digital Imaging SystemsOlicon Imaging Systems, Inc.1993—
−5K973959Olicon Imaging Systems, Inc. 02-Workstation and/or Pacsview SoftwareOlicon Imaging Systems, Inc.1997—
−4K043146Horizon Medical ImagingMckesson Medical Imaging Company200511
−3K152186HealthMyne PACSHealthmyne, Inc.2015—
−2K171544Arterys ViewerArterys, Inc.2017—
−1K211257EFAI PACS Picture Archiving and Communication SystemEver Fortune.Ai, Co., Ltd.2021—
0 (this device)K232100Efai Pacs Picture Archiving and Communication System ProEver Fortune.Ai, Co., Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
199310
199810
200210
FIG. 1 — Lineage of K232100, 1993–2023Source: 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 LLZ? 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 LLZ device

  1. #1 K230955 syngo Application Softwarescore 21.5 · 11 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
*K211257EFAI PACS Picture Archiving and Communication System
Summary page 4
…ry Name EFAI PACS PICTURE ARCHIVING AND COMMUNICATION SYSTEM (EFAI PACS) Premarket Notification K211257 EFAI PACS PRO Special 510(k) 1 Classification Name…
Ever Fortune.Ai, Co., Ltd.2021—

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 30 years and passes through 5 companies; a new generation was cleared every 4.9 years on median.
  • 1 of the 10 ancestors has a recall of any class.

How does its category compare?

All LLZ devices

LLZ System, Image Processing, Radiological: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · LLZ

58in 2025

2007: 762008: 942009: 702010: 512011: 1062012: 822013: 952014: 782015: 642016: 822017: 782018: 1042019: 742020: 812021: 832022: 652023: 872024: 622025: 582026 (partial year): 45
2007high 106 (2011) · low 51 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LLZ

173in 2025

2007: 36 days median2008: 52 days median2009: 62 days median2010: 98 days median2011: 79 days median2012: 87 days median2013: 84 days median2014: 89 days median2015: 90 days median2016: 90 days median2017: 107 days median2018: 105 days median2019: 107 days median2020: 115 days median2021: 116 days median2022: 137 days median2023: 157 days median2024: 131 days median2025: 173 days median2026 (partial year): 110 days median
2007high 173 (2025) · low 36 (2007)2026

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

Recalls per year · LLZ

11in 2025

2007: 202008: 322009: 212010: 172011: 302012: 122013: 642014: 62015: 162016: 122017: 52018: 72019: 22020: 62021: 32022: 42023: 82024: 62025: 112026 (partial year): 14
2007high 64 (2013) · low 2 (2019)2026

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

Adverse event reports per year · LLZ

116in 2025

2007: 1522008: 1542009: 1452010: 1452011: 4542012: 2662013: 1,1302014: 15,6312015: 2112016: 2902017: 1042018: 722019: 882020: 822021: 702022: 282023: 262024: 422025: 116
2007high 15,631 (2014) · low 26 (2023)2025

MAUDE reports naming product code LLZ, 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
2007763620152
2008945232154
2009706221145
2010519817145
20111067930454
2012828712266
20139584641,130
20147889615,631
2015649016211
2016829012290
2017781075104
2018104105772
201974107288
202081115682
202183116370
202265137428
202387157826
202462131642
20255817311116
20264511014—

What is it indicated for?

EFAI PACS PRO is intended to be used as a Digital Imaging and Communications in Medicine (DICOM) and non-DICOM information and data management system. The EFAI PACS PRO displays, processes, stores, and transfers medical data from original equipment manufacturers (OEMs) that support the DICOM standard, with the exception of mammography. It provides the capability to store images and patient information from OEM equipment, and perform filtering, digital…

Read the full statement (136 words)

EFAI PACS PRO is intended to be used as a Digital Imaging and Communications in Medicine (DICOM) and non-DICOM information and data management system. The EFAI PACS PRO displays, processes, stores, and transfers medical data from original equipment manufacturers (OEMs) that support the DICOM standard, with the exception of mammography. It provides the capability to store images and patient information from OEM equipment, and perform filtering, digital manipulation and quantitative measurements. The client software is designed to run on standard personal and business computers. The product is intended to be used by trained medical professionals, including but not limited to radiologists, oncologists, and physicians. It is intended to provide image and related information that is interpreted by a trained professional to render findings and/or diagnosis, but it does not directly generate any diagnosis or potential findings.

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. “K232100: Efai Pacs Picture Archiving and Communication System Pro.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K232100

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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