510(k) Report

510(k) · Cleared

Cleared

THE Graft Collagen

K230305510(k) TraditionalCleared Jul 24, 2024537-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

Purgo Biologics, Inc. · NPM Bone Grafting Material, Animal Source

Cleared on Jul 24, 2024 as substantially equivalent to K122894 (Geistlich Pharma AG, 2013) after a 537-day review. Its family tree reaches back 6 generations to 1995.

Decided
Jul 24, 2024
Review
537 days
Class
Class II
Product code
NPM
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K924408 (1995). 16 ancestors in all, the oldest K871773 (1987). No later device cites it as a predicate yet.

  1. Root · 6 generations backK924408 Colla-Tec Absorbable Collagen MembraneColla-Tec, Inc. · 1995 · Recalled
  2. 5 generations backK992216 Biomend Extend Absorbable Collagen Membrane, Biomend Absorbable…Integra Lifesciences Corp. · 1999 · Recalled
  3. 4 generations backK042197 Bio-Gide Resorbable Bilayer Membrane for Guided Tissue and Bone…Ed. Geistlich Soehne AG Fuer Chemische Industrie · 2004
  4. 3 generations backK050446 Bio-Gide Resorbable Bilayer Membrane for Guided Tissue and BoneEd. Geistlich Soehne AG Fuer Chemische Industrie · 2005
  5. 2 generations backK112572 Geistlich Combi-Kit CollegenGeistlich Pharma AG · 2011
  6. 1 generation backK122894 Geistlich Bio-Oss, Geistlich Bio-Oss Collagen, Geistlich Combi-Kit…Geistlich Pharma AG · 2013
  7. This deviceK230305 THE Graft CollagenPurgo Biologics, Inc. · 2024
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K924408Colla-Tec Absorbable Collagen MembraneColla-Tec, Inc.19952
−5K992216Biomend Extend Absorbable Collagen Membrane, Biomend Absorbable Collagen…Integra Lifesciences Corp.19991
−4K042197Bio-Gide Resorbable Bilayer Membrane for Guided Tissue and Bone RegenerationEd. Geistlich Soehne AG Fuer Chemische Industrie2004—
−3K050446Bio-Gide Resorbable Bilayer Membrane for Guided Tissue and BoneEd. Geistlich Soehne AG Fuer Chemische Industrie2005—
−2K112572Geistlich Combi-Kit CollegenGeistlich Pharma AG2011—
−1K122894Geistlich Bio-Oss, Geistlich Bio-Oss Collagen, Geistlich Combi-Kit Collagen…Geistlich Pharma AG2013—
0 (this device)K230305THE Graft CollagenPurgo Biologics, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198710
199210
199520
199710
199820
200010
200410
201010
FIG. 1 — Lineage of K230305, 1995–2024Source: 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 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
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
*K122894Geistlich Bio-Oss, Geistlich Bio-Oss Collagen, Geistlich Combi-Kit Collagen, Geistlich…
Summary page 5
…ing Material, Animal Source Device class : Class II Classification Panel : Dental 3. Predicate Device Primary predicate device K122894 Bio-Oss® Collagen Reference predicate device K173188 The Graft Bone Substitute 510(k) Summary…
Geistlich Pharma AG2013—
†K173188The Graft Natural Bone SubstitutePurgo Biologics, Inc.2018—

Also cleared against K122894: 9 other devices →

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 29 years and passes through 5 companies; a new generation was cleared every 5.3 years on median.
  • 2 of the 16 ancestors have a recall of any class.
  • 9 other devices also cite its predicate K122894.

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. 2024, 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?

THE Graft Collagen is recommended for:

- Filling of extraction sockets to enhance preservation of the alveolar ridge.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K230305: THE Graft Collagen.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K230305

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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