510(k) Report

510(k) · Cleared

Cleared

MBCP

K051885510(k) TraditionalCleared Sep 16, 200566-day reviewClass II21 CFR 872.3930

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

Biomatlante · LYC Bone Grafting Material, Synthetic

Cleared on Sep 16, 2005 as substantially equivalent to K032268 (Biomatlante, 2003) and 1 other predicate after a 66-day review. Its family tree reaches back 4 generations to 1999. 59 later devices descend from it.

Decided
Sep 16, 2005
Review
66 days
Class
Class II
Product code
LYC
Recalls
None
Predicates
2

Its longest line of descent runs back 4 generations to K990131 (1999). 5 ancestors in all. 59 later devices descend from it, 14 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2000: 1 other ancestor2008: 3 descendants cleared2011: 1 descendant cleared2009: 7 descendants cleared2010: 6 descendants cleared2016: 1 descendant cleared2007: 1 descendant cleared2006: 1 descendant cleared2025: 5 descendants cleared2012: 2 descendants cleared2014: 2 descendants cleared2018: 4 descendants cleared2019: 2 descendants cleared2021: 7 descendants cleared2026: 5 descendants cleared2023: 4 descendants cleared2022: 4 descendants cleared2024: 4 descendants clearedK990131 · Pro Osteon Implant 500R Resorbable Bone Graft Substitute · Interpore Cross Intl. · 1999K020986 · Mastergraft Resorbable Ceramic · Medtronic Sofamor Danek, Inc. · 2002K032268 · MBCP · Biomatlante · 2003K043005 · Modification to MBCP · Biomatlante · 20051995200020052010201520202025
Other ancestors, by generationDescendants, by generation 2 generations back: 1 other ancestor 1 generation forward: 14 descendants2 generations forward: 7 descendants3 generations forward: 13 descendants4 generations forward: 13 descendants5 generations forward: 9 descendants6 generations forward: 3 descendants K043005 · Modification to MBCP · Biomatlante · 2005K032268 · MBCP · Biomatlante · 2003K020986 · Mastergraft Resorbable Ceramic · Medtronic Sofamor Danek, Inc. · 2002K990131 · Pro Osteon Implant 500R Resorbable Bone Graft Substitute · Interpore Cross Intl. · 19990+5
  1. Root · 4 generations backK990131 Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl. · 1999
  2. 3 generations backK020986 Mastergraft Resorbable CeramicMedtronic Sofamor Danek, Inc. · 2002
  3. 2 generations backK032268 MBCPBiomatlante · 2003
  4. 1 generation backK043005 Modification to MBCPBiomatlante · 2005
  5. This deviceK051885 MBCPBiomatlante · 2005
  6. Descendant · cites it directly · 40 of its ownK060732 MBCP GelBiomatlante · 2006
  7. Descendant · 2 generations on · 37 of its ownK080917 Iroot SPInnovative Bioceramix, Inc. · 2008
  8. Descendant · 3 generations on · 12 of its ownK082943 Iroot BP, Model Irbp 4609Innovative Bioceramix, Inc. · 2009
  9. Descendant · 3 generations on · 8 of its ownK170175 Endoseal MtaMaruchi · 2018
  10. Descendant · 4 generations on · 7 of its ownK092715 Iroot BP PlusInnovative Bioceramix, Inc. · 2009

Showing 5 of 59 descendants. See all descendants

Descendants cleared per year

2006: 12007: 12008: 32009: 72010: 62011: 12012: 22014: 22016: 12018: 42019: 22021: 72022: 42023: 42024: 42025: 52026: 5
2006high 7 (2009) · low 0 (2013)2026

Most influential descendants

Showing 5 of 59 · See all
  • K060732MBCP GelBiomatlante · 2006 · cites it directly40descendants
  • K080917Iroot SPInnovative Bioceramix, Inc. · 2008 · 2 generations on37descendants
  • K082943Iroot BP, Model Irbp 4609Innovative Bioceramix, Inc. · 2009 · 3 generations on12descendants
  • K170175Endoseal MtaMaruchi · 2018 · 3 generations on8descendants
  • K092715Iroot BP PlusInnovative Bioceramix, Inc. · 2009 · 4 generations on7descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K990131Pro Osteon Implant 500R Resorbable Bone Graft SubstituteInterpore Cross Intl.1999—
−3K020986Mastergraft Resorbable CeramicMedtronic Sofamor Danek, Inc.2002—
−2K032268MBCPBiomatlante2003—
−1K043005Modification to MBCPBiomatlante2005—
0 (this device)K051885MBCPBiomatlante2005—
+1K060732MBCP GelBiomatlante2006—
+2K080917Iroot SPInnovative Bioceramix, Inc.2008—
+3K082943Iroot BP, Model Irbp 4609Innovative Bioceramix, Inc.2009—
+3K170175Endoseal MtaMaruchi2018—
+4K092715Iroot BP PlusInnovative Bioceramix, Inc.2009—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200610
200710
200830
200970
201060
201110
201220
201420
201610
201840
201920
202170
202240
202340
202440
202550
202650
FIG. 1 — Lineage of K051885, 1999–2026Source: 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 LYC? 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 LYC device

  1. #1 K253317 Cytrans™ Elashieldscore 14.3 · 10 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? (2)

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
*K032268MBCP
Summary page 2
…NTIAL EQUIVALENCE INFORMATION The material composition of MBCPTM Resorbable Bone Graft Substitute for Dental Bone Grafting is the same as previously cleared MBCP TM (K032268, K043005). Intended Use of MBCPTM Bone Graft Substitute is substantially equivalent to the predicates. The safety and effect…
Biomatlante2003—
*K043005Modification to MBCP
Summary page 2
…IVALENCE INFORMATION The material composition of MBCPTM Resorbable Bone Graft Substitute for Dental Bone Grafting is the same as previously cleared MBCP TM (K032268, K043005). Intended Use of MBCPTM Bone Graft Substitute is substantially equivalent to the predicates. The safety and effectiveness o…
Biomatlante2005—

Also cleared against K032268: 10 other devices →

What descends from it? (59)

See all 59

14 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K060732MBCP GelBiomatlante200640
K062834Osteon, Models GBG0305, GBG0510, GBG1020, GBG2030, GBG3040, GBG4050Genoss Co., Ltd.20075
K082917Mastergraft Resorbable Ceramic GranulesMedtronic Sofamor Danek20093
K090950Bone Plus BCPMegagen Implant Co., Ltd.20101
K082286BioactysGraftys20091
K081784Mastergraft PuttyMedtronic Sofamor Danek20081
K244006FG Bone Graft MFull Golden Biotech Co., Ltd.20250
K153676Osteon IiiGenoss Co., Ltd.20160
K103820Reprobone Dental Grafting MaterialCeramisys, Ltd.20110
K093871Periophil B-TCPCytophil, Inc.20100

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 6 years and passes through 3 companies; a new generation was cleared every 1.4 years on median.
  • None of the 5 ancestors has a recall.
  • Of its descendants, K060732 (Biomatlante, 2006) has gone furthest, with 40 descendants of its own.
  • 10 other devices also cite its predicate K032268.

How does its category compare?

All LYC devices

LYC Bone Grafting Material, Synthetic: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LYC

3in 2025

2007: 132008: 82009: 142010: 132011: 92012: 52013: 22014: 12016: 22020: 32022: 22025: 32026 (partial year): 3
2007high 14 (2009) · low 0 (2015)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LYC

267in 2025

2007: 80 days median2008: 73 days median2009: 100 days median2010: 164 days median2011: 224 days median2012: 120 days median2020: 156 days median2025: 267 days median2026 (partial year): 266 days median
2007high 267 (2025) · low 73 (2008)2026

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

Recalls per year · LYC

1in 2018

2009: 12010: 22012: 22016: 22018: 1
2007high 2 (2010) · low 0 (2007)2026

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

Adverse event reports per year · LYC

2in 2025

2007: 232008: 252009: 252010: 282011: 212012: 102013: 122014: 92015: 142016: 1402017: 192018: 142019: 152020: 52021: 122022: 62023: 92024: 62025: 2
2007high 140 (2016) · low 2 (2025)2025

MAUDE reports naming product code LYC, 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
20071380023
2008873025
200914100125
201013164228
20119224021
20125120210
20132—012
20141—09
20150—014
20162—2140
20170—019
20180—114
20190—015
2020315605
20210—012
20222—06
20230—09
20240—06
2025326702
202632660—

What is it indicated for?

MBCPTM is intended for use as a bone grafting material to fill, augment or reconstruct periodontal or oral/maxillofacial defects.

These defects may be surgically created osseous defects or osseous defects created from traumatic injury to the bone.

MBCPTM can be used with autogenous bone grafting materials.

Typical uses include:

* Periodontal/Infrabony defects

* Ridge augmentation

* Extraction sites (implant preparation/placement)

* Sinus lifts

* Cystic cavities

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K051885: MBCP.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K051885

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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