510(k) Report

510(k) · Cleared

Cleared

DIA-ROOT BIO Sealer

K200175510(k) TraditionalCleared Jun 25, 2020154-day reviewClass II21 CFR 872.3820

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

DiaDent Group International · KIF Resin, Root Canal Filling

Cleared on Jun 25, 2020 as substantially equivalent to K170950 (Vericom Co., Ltd., 2017) after a 154-day review. Its family tree reaches back 2 generations to 1996.

Decided
Jun 25, 2020
Review
154 days
Class
Class II
Product code
KIF
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K960548 (1996). No later device cites it as a predicate yet.

  1. Root · 2 generations backK960548 AH Plus Root Canal SealerDentsply Intl. · 1996
  2. 1 generation backK170950 Well-Root STVericom Co., Ltd. · 2017
  3. This deviceK200175 DIA-ROOT BIO SealerDiaDent Group International · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K960548AH Plus Root Canal SealerDentsply Intl.1996—
−1K170950Well-Root STVericom Co., Ltd.2017—
0 (this device)K200175DIA-ROOT BIO SealerDiaDent Group International2020—
FIG. 1 — Lineage of K200175, 1996–2020Source: 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 KIF? 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 KIF device

  1. #1 K250710 Injectable Root Canal Bioceramic Sealer (nRoot…score 14.9 · 9 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
*K170950Well-Root ST
Summary page 4
…KIF Device Class II Device Name DIA-ROOT BIO Sealer 3. Primary Predicate Device 510(k) Number K170950 Applicant Vericom Co., Ltd. Device Name Well-Root ST Regulation Number…
Vericom Co., Ltd.2017—

Also cleared against K170950: 1 other device →

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.

What does this lineage say?

  • The line of descent spans 24 years and passes through 3 companies; a new generation was cleared every 21.7 years on median.
  • None of the 2 ancestors has a recall.
  • 1 other device also cites its predicate K170950.

How does its category compare?

All KIF devices

KIF Resin, Root Canal Filling: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · KIF

7in 2025

2007: 22008: 42009: 52010: 52012: 52013: 22014: 102015: 12016: 52017: 32018: 52019: 72020: 32021: 122022: 32023: 72024: 82025: 72026 (partial year): 7
2007high 12 (2021) · low 0 (2011)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KIF

90in 2025

2008: 31 days median2009: 94 days median2010: 75 days median2012: 172 days median2014: 220 days median2016: 212 days median2017: 211 days median2018: 147 days median2019: 252 days median2020: 239 days median2021: 89 days median2022: 152 days median2023: 59 days median2024: 96 days median2025: 90 days median2026 (partial year): 108 days median
2007high 252 (2019) · low 31 (2008)2026

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

Recalls per year · KIF

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

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

Adverse event reports per year · KIF

55in 2025

2008: 22009: 72010: 102011: 82012: 42013: 792014: 4212015: 152016: 52017: 52018: 132019: 62020: 32021: 92022: 102023: 72024: 102025: 55
2007high 421 (2014) · low 0 (2007)2025

MAUDE reports naming product code KIF, 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
20072—00
200843102
200959417
2010575010
20110—08
2012517204
20132—079
2014102200421
20151—015
2016521205
2017321105
20185147013
2019725206
2020323903
2021128909
20223152010
202375907
2024896010
2025790055
202671080—

What is it indicated for?

DIA-ROOT BIO Sealer is a MTA (mineral trioxide aggregate) based root canal sealer that provides complete and permanent sealing of root canals. It can be used with or without root canal obturation materials.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K200175: DIA-ROOT BIO Sealer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K200175

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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