510(k) Report

510(k) · Cleared

Cleared

Bioceramic Root Repair Material (C-Root BP)

K240365510(k) TraditionalCleared May 10, 202494-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

Beijing C-Root Dental Medical Devices Co., Ltd. · KIF Resin, Root Canal Filling

Cleared on May 10, 2024 as substantially equivalent to K092715 (Innovative Bioceramix, Inc., 2009) after a 94-day review. Its family tree reaches back 9 generations to 1999. 1 later device descends from it.

Decided
May 10, 2024
Review
94 days
Class
Class II
Product code
KIF
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K990131 (1999). 36 ancestors in all, the oldest K852682 (1985). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 1 other ancestor2005: 1 other ancestor1988: 1 other ancestor2004: 4 other ancestors2001: 4 other ancestors1996: 3 other ancestors1993: 2 other ancestors2000: 2 other ancestors1999: 1 other ancestor1989: 2 other ancestors1998: 1 other ancestor1997: 2 other ancestors1995: 2 other ancestors1985: 1 other ancestor2024: 1 descendant clearedReference device: K212983 · Injectable Root Canal Bioceramic Sealer · Beijing C-Root Dental Medical Devices Co., Ltd. · 2021K990131 · Pro Osteon Implant 500R Resorbable Bone Graft Substitute · Interpore Cross Intl. · 1999K020986 · Mastergraft Resorbable Ceramic · Medtronic Sofamor Danek, Inc. · 2002K032268 · MBCP · Biomatlante · 2003×2: 2 generations cleared close together, K043005 (2005), K051885 (2005) K060732 · MBCP Gel · Biomatlante · 2006K080917 · Iroot SP · Innovative Bioceramix, Inc. · 2008K082943 · Iroot BP, Model Irbp 4609 · Innovative Bioceramix, Inc. · 2009K092715 · Iroot BP Plus · Innovative Bioceramix, Inc. · 20091990200020102020
  1. Root · 9 generations backK990131 Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl. · 1999
  2. 5 generations between
  3. 3 generations backK080917 Iroot SPInnovative Bioceramix, Inc. · 2008
  4. 2 generations backK082943 Iroot BP, Model Irbp 4609Innovative Bioceramix, Inc. · 2009
  5. 1 generation backK092715 Iroot BP PlusInnovative Bioceramix, Inc. · 2009
  6. This deviceK240365 Bioceramic Root Repair Material (C-Root BP)Beijing C-Root Dental Medical Devices Co., Ltd. · 2024
  7. Descendant · cites it directly · 0 of its ownK242934 Bioceramic Root Canal Sealer and Repair Materials (i-MTA BP)Longly Biotechnology (Wuhan) Co., Ltd. · 2024
Show all 9 generations
  1. Root · 9 generations backK990131 Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl. · 1999
  2. 8 generations backK020986 Mastergraft Resorbable CeramicMedtronic Sofamor Danek, Inc. · 2002
  3. 7 generations backK032268 MBCPBiomatlante · 2003
  4. 6 generations backK043005 Modification to MBCPBiomatlante · 2005
  5. 5 generations backK051885 MBCPBiomatlante · 2005
  6. 4 generations backK060732 MBCP GelBiomatlante · 2006
  7. 3 generations backK080917 Iroot SPInnovative Bioceramix, Inc. · 2008
  8. 2 generations backK082943 Iroot BP, Model Irbp 4609Innovative Bioceramix, Inc. · 2009
  9. 1 generation backK092715 Iroot BP PlusInnovative Bioceramix, Inc. · 2009
  10. This deviceK240365 Bioceramic Root Repair Material (C-Root BP)Beijing C-Root Dental Medical Devices Co., Ltd. · 2024

Most influential descendants

Showing 1 of 1 · See all
  • K242934Bioceramic Root Canal Sealer and Repair Materials (i-MTA BP)Longly Biotechnology (Wuhan) Co., Ltd. · 2024 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K990131Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl.1999—
−8K020986Mastergraft Resorbable CeramicMedtronic Sofamor Danek, Inc.2002—
−7K032268MBCPBiomatlante2003—
−6K043005Modification to MBCPBiomatlante2005—
−5K051885MBCPBiomatlante2005—
−4K060732MBCP GelBiomatlante2006—
−3K080917Iroot SPInnovative Bioceramix, Inc.2008—
−2K082943Iroot BP, Model Irbp 4609Innovative Bioceramix, Inc.2009—
−1K092715Iroot BP PlusInnovative Bioceramix, Inc.2009—
0 (this device)K240365Bioceramic Root Repair Material (C-Root BP)Beijing C-Root Dental Medical Devices Co., Ltd.2024—
+1K242934Bioceramic Root Canal Sealer and Repair Materials (i-MTA BP)Longly Biotechnology (Wuhan) Co., Ltd.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198510
198810
198920
199320
199520
199630
199720
199810
199910
200020
200140
200440
200510
200610

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202410
FIG. 1 — Lineage of K240365, 1999–2024Source: 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
Get a 510(k) Report

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
*K092715Iroot BP Plus
Summary page 5
…tal Manufacturer: Beijing C-Root Dental Medical Devices Co., LTD. 3.0 Identification of Predicated Device and Reference device Primary Predicate Device: 510(k) Number: K092715 1/8 510(k) Summary Product Name: iRoot BP Plus Common Name:Bioceramic Root Repair Material Production code:KIF…
Innovative Bioceramix, Inc.2009—
†K212983Injectable Root Canal Bioceramic SealerBeijing C-Root Dental Medical Devices Co., Ltd.2021—

Also cleared against K092715: 4 other devices →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K242934Bioceramic Root Canal Sealer and Repair Materials (i-MTA BP)Longly Biotechnology (Wuhan) Co., Ltd.20240

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 25 years and passes through 5 companies; a new generation was cleared every 1.4 years on median.
  • None of the 36 ancestors has a recall.
  • Of its descendants, K242934 (Longly Biotechnology (Wuhan) Co., Ltd., 2024) has gone furthest, with 0 descendants of its own.
  • 4 other devices also cite its predicate K092715.

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. 2024, 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?

*Repair of Root Perforation

*Repair of Root Resorption

*Root End Filling

*Apexification

*Pulp Capping

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K240365: Bioceramic Root Repair Material (C-Root BP).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K240365

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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