510(k) Report

510(k) · Cleared

Cleared

Ultima 2 Dental Chair

K942870510(k) TraditionalCleared Feb 27, 1995255-day reviewClass I21 CFR 872.6250

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

Dentech Corp. · KLC Chair, Dental, With Operative Unit

Cleared on Feb 27, 1995 after a 255-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

Decided
Feb 27, 1995
Review
255 days
Class
Class I
Product code
KLC
Recalls
None
Predicates
0

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

FIG. 1 — Lineage of K942870Source: FDA 510(k) database · 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 KLC? 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 KLC device

  1. #1 K233921 Luvis Chair (LC700C)score 11.9 · 4 generations · no Class I recall
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What was it cleared against?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

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.

How does its category compare?

All KLC devices

KLC Chair, Dental, With Operative Unit: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KLC

1in 2024

2007: 12016: 12024: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KLC

Too few KLC 510(k)s in any year since 2007 to give a median.

Recalls per year · KLC

6in 2010

2009: 12010: 6
2007high 6 (2010) · low 0 (2007)2026

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

Adverse event reports per year · KLC

1in 2022

2007: 12008: 22009: 12010: 12011: 72012: 12013: 12014: 22015: 12022: 1
2007high 7 (2011) · low 0 (2016)2025

MAUDE reports naming product code KLC, 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—01
20080—02
20090—11
20100—61
20110—07
20120—01
20130—01
20140—02
20150—01
20161—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—01
20230—00
20241—00
20250—00
20260—0—
Cite this page

510(k) Report. “K942870: Ultima 2 Dental Chair.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K942870

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