510(k) Report

510(k) · Cleared

Recalled · Class III · 2018

Porcine Anorganic Bone Mineral

K140714510(k) TraditionalCleared Jul 16, 2014117-day reviewClass II21 CFR 872.3930Recalls 2

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

Collagen Matrix, Inc. · NPM Bone Grafting Material, Animal Source

Cleared on Jul 16, 2014 as substantially equivalent to K043034 (Collagen Matrix, Inc., 2005) and 1 other predicate after a 117-day review. Its family tree reaches back 3 generations to 1987. 4 later devices descend from it. It has been recalled 2 times.

Decided
Jul 16, 2014
Review
117 days
Class
Class II
Product code
NPM
Recalls
2
Predicates
2

Its longest line of descent runs back 3 generations to K871773 (1987). 9 ancestors in all. 4 later devices descend from it, 3 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 1995: 2 other ancestors2000: 1 other ancestor1998: 2 other ancestors1992: 1 other ancestor2018: 1 descendant cleared2017: 1 descendant cleared2020: 2 descendants clearedK871773 · Bio-Oss Pure Nat Hydroxyapatite Endoss Implant · Geistlich-Pharma · 1987K033815 · Bio-Oss, Bio-Oss Blocks and Bio-Oss Collagen · Geistlich-Pharma · 2004K043034 · Osteoguide Anorganic Bone Mineral Products · Collagen Matrix, Inc. · 2005 · recalled1990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 3 other ancestors 1 generation forward: 3 descendants2 generations forward: 1 descendant K043034 · Osteoguide Anorganic Bone Mineral Products · Collagen Matrix, Inc. · 2005 · recalledK033815 · Bio-Oss, Bio-Oss Blocks and Bio-Oss Collagen · Geistlich-Pharma · 2004K871773 · Bio-Oss Pure Nat Hydroxyapatite Endoss Implant · Geistlich-Pharma · 19870
  1. Root · 3 generations backK871773 Bio-Oss Pure Nat Hydroxyapatite Endoss ImplantGeistlich-Pharma · 1987
  2. 2 generations backK033815 Bio-Oss, Bio-Oss Blocks and Bio-Oss CollagenGeistlich-Pharma · 2004
  3. 1 generation backK043034 Osteoguide Anorganic Bone Mineral ProductsCollagen Matrix, Inc. · 2005 · Recalled
  4. This deviceK140714 Porcine Anorganic Bone MineralCollagen Matrix, Inc. · 2014
  5. Descendant · cites it directly · 1 of its ownK173188 The Graft Natural Bone SubstitutePurgo Biologics, Inc. · 2018
  6. Descendant · cites it directly · 1 of its ownK162158 Porcine Anorganic Bone Mineral in Delivery ApplicatorCollagen Matrix, Inc. · 2017
  7. Descendant · cites it directly · 0 of its ownK201859 Porcine Mineral Collagen Composite MoldableCollagen Matrix, Inc. · 2020
  8. Descendant · 2 generations on · 0 of its ownK191737 The Graft Bone SubstitutePurgo Biologics, Inc. · 2020

Most influential descendants

Showing 4 of 4 · See all
  • K173188The Graft Natural Bone SubstitutePurgo Biologics, Inc. · 2018 · cites it directly1descendant
  • K162158Porcine Anorganic Bone Mineral in Delivery ApplicatorCollagen Matrix, Inc. · 2017 · cites it directly1descendant
  • K201859Porcine Mineral Collagen Composite MoldableCollagen Matrix, Inc. · 2020 · cites it directly0descendants
  • K191737The Graft Bone SubstitutePurgo Biologics, Inc. · 2020 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K871773Bio-Oss Pure Nat Hydroxyapatite Endoss ImplantGeistlich-Pharma1987—
−2K033815Bio-Oss, Bio-Oss Blocks and Bio-Oss CollagenGeistlich-Pharma2004—
−1K043034Osteoguide Anorganic Bone Mineral ProductsCollagen Matrix, Inc.20053
0 (this device)K140714Porcine Anorganic Bone MineralCollagen Matrix, Inc.2014—
+1K173188The Graft Natural Bone SubstitutePurgo Biologics, Inc.2018—
+1K162158Porcine Anorganic Bone Mineral in Delivery ApplicatorCollagen Matrix, Inc.2017—
+1K201859Porcine Mineral Collagen Composite MoldableCollagen Matrix, Inc.2020—
+2K191737The Graft Bone SubstitutePurgo Biologics, Inc.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199210
199520
199820
200010

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
201810
202020
FIG. 1 — Lineage of K140714, 1987–2020Source: 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 NPM? 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 NPM device

  1. #1 K240661 Geistlich Bio-Oss®score 15.2 · 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? (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
*K043034Osteoguide Anorganic Bone Mineral Products
Summary page 1
…d Devices to Which Substantial Equivalence is Claimed Predicate Device(s): OsteoGuidem Anorganic Bone Mineral K043034 Bio-Oss®D Granules K952617 14. Description of th…
Collagen Matrix, Inc.20053
*K952617Bio-Oss
Summary page 1
…Anorganic Bone Mineral K043034 Bio-Oss®D Granules K952617 14. Description of the Device Porcine Anorganic Bone Mineral is a porous bone graft material consisting predominantly o…
Geistlich-Pharma1995—

Also cleared against K043034: 8 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K173188The Graft Natural Bone SubstitutePurgo Biologics, Inc.20181
K162158Porcine Anorganic Bone Mineral in Delivery ApplicatorCollagen Matrix, Inc.20171
K201859Porcine Mineral Collagen Composite MoldableCollagen Matrix, Inc.20200

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Oct 30, 2018Class IIIZ-0752-2019Employee errorThere is a possibility that the product labeled as 4.0cc volume may only contain 2.0cc volume and is therefore mislabeled.
Nov 17, 2015Class IIIZ-1173-2016Component design/selectionThe distributor, Osteogenics Biomedical, notified the firm that the syringes were not working properly and the syringes were being held in quarantine.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 27 years and passes through 2 companies; a new generation was cleared every 8.9 years on median.
  • 1 of the 9 ancestors has a recall of any class.
  • Of its descendants, K173188 (Purgo Biologics, Inc., 2018) has gone furthest, with 1 descendant of its own.
  • 8 other devices also cite its predicate K043034.

How does its category compare?

All NPM devices

NPM Bone Grafting Material, Animal Source: FDA decisions, review times, recalls and adverse event reports over 20 years. 2014, this device’s year, is highlighted.

FDA decisions per year · NPM

3in 2025

2009: 12010: 22011: 32012: 22013: 22014: 22015: 42016: 12017: 52018: 22020: 32021: 22023: 22024: 32025: 32026 (partial year): 3
2007high 5 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NPM

30in 2025

2011: 112 days median2015: 349 days median2017: 191 days median2020: 231 days median2024: 211 days median2025: 30 days median2026 (partial year): 269 days median
2007high 349 (2015) · low 30 (2025)2026

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

Recalls per year · NPM

1in 2022

2018: 12020: 32022: 1
2007high 3 (2020) · low 0 (2007)2026

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

Adverse event reports per year · NPM

14in 2025

2007: 12010: 12012: 22013: 32014: 32015: 12016: 12017: 32018: 82019: 62020: 32021: 42022: 272023: 42024: 52025: 14
2007high 27 (2022) · low 0 (2008)2025

MAUDE reports naming product code NPM, 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
20070—01
20080—00
20091—00
20102—01
2011311200
20122—02
20132—03
20142—03
2015434901
20161—01
2017519103
20182—18
20190—06
2020323133
20212—04
20220—127
20232—04
2024321105
2025330014
202632690—

What is it indicated for?

Porcine Anorganic Bone Mineral is intended for use in dental surgery. The products may be used in surgical procedures such as:

* Augmentation or reconstructive treatment of alveolar ridge

* Filling of infrabony periodontal defects

* Filling of defects after root resection, apicoectomy, and cystectomy

* Filling of extraction sockets to enhance preservation of the alveolar ridge

* Elevation of maxillary sinus floor

* Filling of periodontal defects in conjunction with products intended for Guided Tissue Regeneration (GTR) and Guided Bone Regeneration (GBR)

* Filling of peri-implant defects in conjunction with products intended for Guided Bone Regeneration.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K140714: Porcine Anorganic Bone Mineral.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K140714

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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