510(k) Report

510(k) · Cleared

Cleared

Oralix Pan DC Iii Ceph or Panoramic Mode Only

K880982510(k) TraditionalCleared Jun 6, 198890-day reviewClass II21 CFR 892.1680

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

Orion Corporation Soredex · KPR System, X-Ray, Stationary

Cleared on Jun 6, 1988 after a 90-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jun 6, 1988
Review
90 days
Class
Class II
Product code
KPR
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 1998: 1 descendant cleared1990200020102020
  1. This deviceK880982 Oralix Pan DC Iii Ceph or Panoramic Mode OnlyOrion Corporation Soredex · 1988
  2. Descendant · cites it directly · 0 of its ownK974877 Cranex Tome Ceph, or Cranex TomeOrion Corporation Soredex · 1998 · Recalled

Most influential descendants

Showing 1 of 1 · See all
  • K974877Cranex Tome Ceph, or Cranex TomeOrion Corporation Soredex · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K880982Oralix Pan DC Iii Ceph or Panoramic Mode OnlyOrion Corporation Soredex1988—
+1K974877Cranex Tome Ceph, or Cranex TomeOrion Corporation Soredex19981

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
FIG. 1 — Lineage of K880982, 1988–1998Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KPR? 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 KPR device

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K974877Cranex Tome Ceph, or Cranex TomeOrion Corporation Soredex19980

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, K974877 (Orion Corporation Soredex, 1998) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KPR devices

KPR System, X-Ray, Stationary: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KPR

8in 2025

2007: 122008: 152009: 92010: 92011: 92012: 112013: 52014: 102015: 182016: 112017: 62018: 152019: 122020: 162021: 62022: 82023: 92024: 112025: 82026 (partial year): 6
2007high 18 (2015) · low 5 (2013)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPR

155in 2025

2007: 31 days median2008: 48 days median2009: 35 days median2010: 126 days median2011: 152 days median2012: 58 days median2013: 163 days median2014: 108 days median2015: 81 days median2016: 84 days median2017: 75 days median2018: 30 days median2019: 33 days median2020: 39 days median2021: 55 days median2022: 43 days median2023: 76 days median2024: 162 days median2025: 155 days median2026 (partial year): 197 days median
2007high 197 (2026) · low 30 (2018)2026

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

Recalls per year · KPR

7in 2025

2007: 102008: 102009: 52010: 32011: 52012: 12013: 52014: 82015: 12016: 42017: 32018: 42019: 12020: 12022: 22023: 42024: 12025: 7
2007high 10 (2007) · low 0 (2021)2026

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

Adverse event reports per year · KPR

39in 2025

2007: 1202008: 952009: 612010: 822011: 1032012: 742013: 242014: 342015: 592016: 182017: 312018: 362019: 772020: 412021: 372022: 272023: 392024: 342025: 39
2007high 120 (2007) · low 18 (2016)2025

MAUDE reports naming product code KPR, 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
2007123110120
200815481095
2009935561
20109126382
201191525103
20121158174
20135163524
201410108834
20151881159
20161184418
2017675331
20181530436
20191233177
20201639141
2021655037
2022843227
2023976439
202411162134
20258155739
202661970—
Cite this page

510(k) Report. “K880982: Oralix Pan DC Iii Ceph or Panoramic Mode Only.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K880982

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026