510(k) Report

510(k) · Cleared

Cleared

Eaglesoft Chairside

K982422510(k) TraditionalCleared Sep 30, 199879-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

Eaglesoft, A Patterson Co. · LLZ System, Image Processing, Radiological

Cleared on Sep 30, 1998 after a 79-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 64 later devices descend from it.

Decided
Sep 30, 1998
Review
79 days
Class
Class II
Product code
LLZ
Recalls
None
Predicates
0

64 later devices descend from it, 6 citing it directly.

Descendants, by year cleared 2005: 2 descendants cleared2011: 2 descendants cleared2006: 1 descendant cleared2009: 1 descendant cleared2012: 1 descendant cleared2023: 5 descendants cleared2017: 3 descendants cleared2010: 1 descendant cleared2014: 2 descendants cleared2007: 1 descendant cleared2016: 2 descendants cleared2022: 6 descendants cleared2025: 8 descendants cleared2015: 1 descendant cleared2013: 2 descendants cleared2021: 4 descendants cleared2018: 3 descendants cleared2019: 2 descendants cleared2020: 5 descendants cleared2026: 8 descendants cleared2024: 4 descendants cleared1995200020052010201520202025
  1. This deviceK982422 Eaglesoft ChairsideEaglesoft, A Patterson Co. · 1998
  2. Descendant · cites it directly · 28 of its ownK061035 Tigerview ProfessionalTelevere Systems · 2006
  3. Descendant · cites it directly · 25 of its ownK043104 Kodak Orthodontic Imaging and Oms Imaging 8.0Practiceworks, Inc. · 2005
  4. Descendant · 2 generations on · 22 of its ownK122427 CS Orthodontic Imaging Software CS Oms Imaging SoftwareCarestream Dental, LLC · 2012
  5. Descendant · 3 generations on · 19 of its ownK131570 OrthovisionEwoosoft Co., Ltd. · 2013
  6. Descendant · 4 generations on · 18 of its ownK173094 OrthoVisionEwoosoft Co., Ltd. · 2017

Showing 5 of 64 descendants. See all descendants

Descendants cleared per year

2005: 22006: 12007: 12009: 12010: 12011: 22012: 12013: 22014: 22015: 12016: 22017: 32018: 32019: 22020: 52021: 42022: 62023: 52024: 42025: 82026: 8
2005high 8 (2025) · low 0 (2008)2026

Most influential descendants

Showing 5 of 64 · See all
  • K061035Tigerview ProfessionalTelevere Systems · 2006 · cites it directly28descendants
  • K043104Kodak Orthodontic Imaging and Oms Imaging 8.0Practiceworks, Inc. · 2005 · cites it directly25descendants
  • K122427CS Orthodontic Imaging Software CS Oms Imaging SoftwareCarestream Dental, LLC · 2012 · 2 generations on22descendants
  • K131570OrthovisionEwoosoft Co., Ltd. · 2013 · 3 generations on19descendants
  • K173094OrthoVisionEwoosoft Co., Ltd. · 2017 · 4 generations on18descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K982422Eaglesoft ChairsideEaglesoft, A Patterson Co.1998—
+1K061035Tigerview ProfessionalTelevere Systems2006—
+1K043104Kodak Orthodontic Imaging and Oms Imaging 8.0Practiceworks, Inc.2005—
+2K122427CS Orthodontic Imaging Software CS Oms Imaging SoftwareCarestream Dental, LLC2012—
+3K131570OrthovisionEwoosoft Co., Ltd.2013—
+4K173094OrthoVisionEwoosoft Co., Ltd.2017—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200520
200610
200710
200910
201010
201120
201210
201320
201420
201510
201620
201730
201830
201920
202050
202140
202260
202350
202440
202580
202680
FIG. 1 — Lineage of K982422, 1998–2026Source: 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 510(k) statement (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?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it? (64)

See all 64

6 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K061035Tigerview ProfessionalTelevere Systems200628
K043104Kodak Orthodontic Imaging and Oms Imaging 8.0Practiceworks, Inc.200525
K082623Visix ImagingTelevere Systems20099
K112974Picture Archiving and Communications SystemCurve Dental, Inc.20117
K053010Vistadent at Complete, Model 3.1Dentsply Intl., Inc.20051
K110139Curve ImageCurve Dental, Inc.20110

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?

  • Of its descendants, K061035 (Televere Systems, 2006) has gone furthest, with 28 descendants of its own.

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.

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?

EagleSoft's ChairSide is a clinical software program that enables dental offices to keep records of hard and soft tissue charts, treatment plans, clinical notes, audio recordings, and clinical exam data. In addition, it also offers an imaging module for image acquisition, editing, and storage of digital images. It is designed to be a single-source solution for a dentist's software needs for clinical and diagnostic use when serving the general public.…

Read the full statement (113 words)

EagleSoft's ChairSide is a clinical software program that enables dental offices to keep records of hard and soft tissue charts, treatment plans, clinical notes, audio recordings, and clinical exam data. In addition, it also offers an imaging module for image acquisition, editing, and storage of digital images. It is designed to be a single-source solution for a dentist's software needs for clinical and diagnostic use when serving the general public.

Images can be acquired from standard dental imaging devices including Digital Radiographic Devices, Digital Video Capture Devices, and Generic Image Devices such as scanners. Non-diagnostic images can then be edited (i.e. resized, contrast, cropped, etc.). Images can also be easily imported and exported.

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K982422: Eaglesoft Chairside.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K982422

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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