510(k) Report

510(k) · Cleared

Cleared

Dental Unit

K142206510(k) TraditionalCleared Mar 13, 2015214-day reviewClass I21 CFR 872.6640

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

Zhuhai Siger Medical Equipment Co., Ltd. · EIA Unit, Operative Dental

Cleared on Mar 13, 2015 as substantially equivalent to K130410 (Xianyang North West Medical Instrument (Group) Co., 2013) after a 214-day review. Its family tree reaches back 5 generations to 1996. 3 later devices descend from it.

Decided
Mar 13, 2015
Review
214 days
Class
Class I
Product code
EIA
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K962071 (1996). 3 later devices descend from it, 1 citing it directly.

  1. Root · 5 generations backK962071 Spirit S1/S2Pelton & Crane Co. · 1996
  2. 4 generations backK983242 Sirona C8 Dental Operative Unit with AccessoriesSirona Dental Systems GmbH · 1998
  3. 3 generations backK032543 Sirona Dental Systems C8+Dental Operative Unit with AccessoriesSirona Dental Systems GmbH · 2003
  4. 2 generations backK080438 Dental Unit with ChairNorth West Medical Instrument (Group) Co., Ltd. · 2008
  5. 1 generation backK130410 Dental Unit with ChairXianyang North West Medical Instrument (Group) Co. · 2013
  6. This deviceK142206 Dental UnitZhuhai Siger Medical Equipment Co., Ltd. · 2015
  7. Descendant · cites it directly · 2 of its ownK231845 Dental unit Model: MareFoshan Safety Medical Equipment Co., Ltd. · 2024
  8. Descendant · 2 generations on · 0 of its ownK242611 Integral Dental UnitsMipont Medical Equipment Co., Ltd. · 2025
  9. Descendant · 2 generations on · 0 of its ownK242646 Dental Implant UnitGuilin Aesthedent Medical Instruments Co., Ltd. · 2025

Most influential descendants

Showing 3 of 3 · See all
  • K231845Dental unit Model: MareFoshan Safety Medical Equipment Co., Ltd. · 2024 · cites it directly2descendants
  • K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd. · 2025 · 2 generations on0descendants
  • K242646Dental Implant UnitGuilin Aesthedent Medical Instruments Co., Ltd. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K962071Spirit S1/S2Pelton & Crane Co.1996—
−4K983242Sirona C8 Dental Operative Unit with AccessoriesSirona Dental Systems GmbH1998—
−3K032543Sirona Dental Systems C8+Dental Operative Unit with AccessoriesSirona Dental Systems GmbH2003—
−2K080438Dental Unit with ChairNorth West Medical Instrument (Group) Co., Ltd.2008—
−1K130410Dental Unit with ChairXianyang North West Medical Instrument (Group) Co.2013—
0 (this device)K142206Dental UnitZhuhai Siger Medical Equipment Co., Ltd.2015—
+1K231845Dental unit Model: MareFoshan Safety Medical Equipment Co., Ltd.2024—
+2K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd.2025—
+2K242646Dental Implant UnitGuilin Aesthedent Medical Instruments Co., Ltd.2025—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
202520
FIG. 1 — Lineage of K142206, 1996–2025Source: 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 EIA? 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 EIA device

  1. #1 K231845 Dental unit Model: Marescore 14.4 · 6 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K130410Dental Unit with Chair
Summary page 5
…rained dentists and/or dental technicians and assistants. This product is attached with a dental chair.” 5. Predicate Device Identification 510(k) Number: K130410 Product Name: Dental Unit with Chair S2310 Manufacturer: Xianyang North West Medical Instrument (Group) Co., Ltd 6. D…
Xianyang North West Medical Instrument (Group) Co.2013—

What descends from it? (3)

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

NumberDeviceApplicantDecidedDescendants
K231845Dental unit Model: MareFoshan Safety Medical Equipment Co., Ltd.20242

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 19 years and passes through 5 companies; a new generation was cleared every 4.4 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K231845 (Foshan Safety Medical Equipment Co., Ltd., 2024) has gone furthest, with 2 descendants of its own.

How does its category compare?

All EIA devices

EIA Unit, Operative Dental: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · EIA

7in 2025

2007: 32008: 62009: 32010: 32011: 52012: 22013: 22014: 22015: 72016: 42017: 12018: 22019: 22020: 12022: 32023: 32024: 32025: 72026 (partial year): 2
2007high 7 (2015) · low 0 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · EIA

178in 2025

2007: 90 days median2008: 72 days median2009: 109 days median2010: 270 days median2011: 150 days median2015: 214 days median2016: 182 days median2022: 265 days median2023: 686 days median2024: 251 days median2025: 178 days median
2007high 686 (2023) · low 72 (2008)2026

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

Recalls per year · EIA

1in 2013

2012: 12013: 1
2007high 1 (2012) · low 0 (2007)2026

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

Adverse event reports per year · EIA

47in 2025

2010: 22011: 32012: 72013: 62014: 2552015: 4522016: 1512017: 642018: 732019: 682020: 482021: 492022: 442023: 532024: 532025: 47
2007high 452 (2015) · low 0 (2007)2025

MAUDE reports naming product code EIA, 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
200739000
200867200
2009310900
2010327002
2011515003
20122—17
20132—16
20142—0255
201572140452
201641820151
20171—064
20182—073
20192—068
20201—048
20210—049
20223265044
20233686053
20243251053
20257178047
20262—0—

What is it indicated for?

The Dental Unit is intended to supply power to and serve as a base for dental devices; and accessories. It is intended for use in the dental clinic /office environment and used by trained dentists and/or dental technicians and assistants. This product is attached with a dental chair.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K142206: Dental Unit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142206

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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