510(k) Report

510(k) · Cleared

Cleared

Yoshida-Panoura 10

K811210510(k) TraditionalCleared Aug 24, 1981112-day review

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

Kaycor Intl., Ltd.

Cleared on Aug 24, 1981 after a 112-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
Aug 24, 1981
Review
112 days
Recalls
None
Predicates
0

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

Descendants, by year cleared 1997: 1 descendant cleared19801990200020102020
  1. This deviceK811210 Yoshida-Panoura 10Kaycor Intl., Ltd. · 1981
  2. Descendant · cites it directly · 0 of its ownK965072 Panoura Ultra Pan and Panoura Ultra Pan/Ceph Panoramic/Cephalometric…Kaycor Intl., Ltd. · 1997

Most influential descendants

Showing 1 of 1 · See all
  • K965072Panoura Ultra Pan and Panoura Ultra Pan/Ceph Panoramic/Cephalometric X-Ray UnitKaycor Intl., Ltd. · 1997 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K811210Yoshida-Panoura 10Kaycor Intl., Ltd.1981—
+1K965072Panoura Ultra Pan and Panoura Ultra Pan/Ceph Panoramic/Cephalometric X-Ray UnitKaycor Intl., Ltd.1997—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
FIG. 1 — Lineage of K811210, 1981–1997Source: 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.

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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
K965072Panoura Ultra Pan and Panoura Ultra Pan/Ceph Panoramic/Cephalometric X-Ray UnitKaycor Intl., Ltd.19970

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, K965072 (Kaycor Intl., Ltd., 1997) has gone furthest, with 0 descendants of its own.
Cite this page

510(k) Report. “K811210: Yoshida-Panoura 10.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K811210

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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