510(k) Report

510(k) · Cleared

Cleared

AXIS Image Management System

K171098510(k) TraditionalCleared May 2, 201719-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

Sonomed, Inc. · NFJ System, Image Management, Ophthalmic

Cleared on May 2, 2017 as substantially equivalent to K090439 (Carl Zeiss Meditec, Inc., 2009) after a 19-day review. Its family tree reaches back 6 generations to 1990. 1 later device descends from it.

Decided
May 2, 2017
Review
19 days
Class
Class II
Product code
NFJ
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K896095 (1990). 9 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 6 generations backK896095 Images-on-Call Teleradiology SystemDevices & Services Co. · 1990
  2. 5 generations backK962699 Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V. · 1996
  3. 4 generations backK982862 Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V. · 1998
  4. 3 generations backK012093 Aetmed Image Processing SoftwareAetmed, S.P.A. · 2001
  5. 2 generations backK013694 Nidek Advanced Vision Information System (Navis)Nidek, Inc. · 2002
  6. 1 generation backK090439 FORUMCarl Zeiss Meditec, Inc. · 2009
  7. This deviceK171098 AXIS Image Management SystemSonomed, Inc. · 2017
  8. Descendant · cites it directly · 0 of its ownK200385 Continuum PacsIntegrated Ophthalmic Systems, Inc. · 2020

Most influential descendants

Showing 1 of 1 · See all
  • K200385Continuum PacsIntegrated Ophthalmic Systems, Inc. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K896095Images-on-Call Teleradiology SystemDevices & Services Co.1990—
−5K962699Radworks Medical Imaging SoftwareApplicare Medical Imaging, B.V.1996—
−4K982862Radworks Medical Imaging Software with Quality Control ModuleApplicare Medical Imaging, B.V.1998—
−3K012093Aetmed Image Processing SoftwareAetmed, S.P.A.2001—
−2K013694Nidek Advanced Vision Information System (Navis)Nidek, Inc.2002—
−1K090439FORUMCarl Zeiss Meditec, Inc.2009—
0 (this device)K171098AXIS Image Management SystemSonomed, Inc.2017—
+1K200385Continuum PacsIntegrated Ophthalmic Systems, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199110
199610
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
FIG. 1 — Lineage of K171098, 1990–2020Source: 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 NFJ? 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 NFJ device

  1. #1 K260694 Zeiss Clinic 360score 15.0 · 12 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
*K090439FORUM
Summary page 5
…data, videos, and images from computerized ophthalmic diagnostic imaging devices. Legally-Marketed Equivalent Devices Carl Zeiss Surgical GmbH FORUM (k090439) Description of the Device AXIS Image Management System is a browser-based ophthalmic image management system designed…
Carl Zeiss Meditec, Inc.2009—

Also cleared against K090439: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K200385Continuum PacsIntegrated Ophthalmic Systems, Inc.20200

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 27 years and passes through 6 companies; a new generation was cleared every 6.3 years on median.
  • None of the 9 ancestors has a recall.
  • Of its descendants, K200385 (Integrated Ophthalmic Systems, Inc., 2020) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K090439.

How does its category compare?

All NFJ devices

NFJ System, Image Management, Ophthalmic: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · NFJ

2in 2024

2007: 12008: 12009: 42011: 22012: 22013: 52014: 22015: 32017: 52018: 72019: 22020: 52021: 22022: 32023: 42024: 22026 (partial year): 2
2007high 7 (2018) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NFJ

85in 2023

2009: 67 days median2013: 73 days median2015: 87 days median2017: 175 days median2018: 84 days median2020: 116 days median2022: 284 days median2023: 85 days median
2007high 284 (2022) · low 67 (2009)2026

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

Recalls per year · NFJ

1in 2024

2010: 22015: 12020: 22022: 12024: 1
2007high 2 (2010) · low 0 (2007)2026

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

Adverse event reports per year · NFJ

2in 2022

2013: 62014: 12015: 22016: 292017: 42019: 22021: 12022: 2
2007high 29 (2016) · low 0 (2007)2025

MAUDE reports naming product code NFJ, 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—00
20081—00
200946700
20100—20
20112—00
20122—00
201357306
20142—01
201538712
20160—029
2017517504
201878400
20192—02
2020511620
20212—01
2022328412
202348500
20242—10
20250—00
20262—0—

What is it indicated for?

Storage, management, and display of patient data, diagnostic data, videos, and images from computerized ophthalmic diagnostic imaging devices.

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. “K171098: AXIS Image Management System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171098

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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