510(k) Report

510(k) · Cleared

Cleared

ArthroTAK Tendon Anchor Kit

K252635510(k) TraditionalCleared May 1, 2026254-day reviewClass II21 CFR 888.3040

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

ArthroTAK, LLC · MBI Fastener, Fixation, Nondegradable, Soft Tissue

Cleared on May 1, 2026 as substantially equivalent to K260004 (Aevumed, Inc., 2026) and 1 other predicate after a 254-day review. Its family tree reaches back 12 generations to 1996. 1 later device descends from it.

Decided
May 1, 2026
Review
254 days
Class
Class II
Product code
MBI
Recalls
None
Predicates
2

Its longest line of descent runs back 12 generations to K961555 (1996). 24 ancestors in all. 1 later device descends from it, 1 citing it directly.

  1. Root · 12 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 8 generations between
  3. 3 generations backK242895 Aevumed PHANTOM Suture AnchorsAevumed, Inc. · 2025
  4. 2 generations backK253040 Aevumed FASE Suture AnchorAevumed, Inc. · 2025
  5. 1 generation backK260004 Aevumed PROTEKT Suture AnchorAevumed, Inc. · 2026
  6. This deviceK252635 ArthroTAK Tendon Anchor KitArthroTAK, LLC · 2026
  7. Descendant · cites it directly · 0 of its ownK262809 ArthroTAK Tendon Anchor KitArthroTAK, LLC · 2026
Show all 12 generations
  1. Root · 12 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 11 generations backK031685 Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc. · 2003 · Recalled
  3. 10 generations backK053344 Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5…Smith & Nephew, Inc. · 2006
  4. 9 generations backK061863 Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc. · 2006
  5. 8 generations backK071177 Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock…Arthrex, Inc. · 2007
  6. 7 generations backK091844 Arthrex Bio-Composite Suturetak AnchorsArthrex, Inc. · 2009
  7. 6 generations backK110660 Arthrex Biocomposite SuturetakArthrex, Inc. · 2011
  8. 5 generations backK140855 Arthrex Suturetak Suture AnchorsArthrex, Inc. · 2014
  9. 4 generations backK223878 Aevumed RAPID Suture AnchorsAevumed, Inc. · 2023
  10. 3 generations backK242895 Aevumed PHANTOM Suture AnchorsAevumed, Inc. · 2025
  11. 2 generations backK253040 Aevumed FASE Suture AnchorAevumed, Inc. · 2025
  12. 1 generation backK260004 Aevumed PROTEKT Suture AnchorAevumed, Inc. · 2026
  13. This deviceK252635 ArthroTAK Tendon Anchor KitArthroTAK, LLC · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K262809ArthroTAK Tendon Anchor KitArthroTAK, LLC · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−12K961555Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc.1996—
−11K031685Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc.20035
−10K053344Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture…Smith & Nephew, Inc.2006—
−9K061863Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc.2006—
−8K071177Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite…Arthrex, Inc.2007—
−7K091844Arthrex Bio-Composite Suturetak AnchorsArthrex, Inc.2009—
−6K110660Arthrex Biocomposite SuturetakArthrex, Inc.2011—
−5K140855Arthrex Suturetak Suture AnchorsArthrex, Inc.2014—
−4K223878Aevumed RAPID Suture AnchorsAevumed, Inc.2023—
−3K242895Aevumed PHANTOM Suture AnchorsAevumed, Inc.2025—
−2K253040Aevumed FASE Suture AnchorAevumed, Inc.2025—
−1K260004Aevumed PROTEKT Suture AnchorAevumed, Inc.2026—
0 (this device)K252635ArthroTAK Tendon Anchor KitArthroTAK, LLC2026—
+1K262809ArthroTAK Tendon Anchor KitArthroTAK, LLC2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199820
200010
200110
200410
200510
200620
201110
201510
201810
202210

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K252635, 1996–2026Source: 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 MBI? 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 MBI device

  1. #1 K203268 Arthrex FiberTak Suture Anchorscore 21.4 · 11 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? (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
*K260004Aevumed PROTEKT Suture Anchor
Cleared while this submission was under review
Summary page 5
…21 CFR 807.92(a)(3) Predicate # Predicate Trade Name (Primary Predicate is listed first) Product Code K260004 Aevumed PROTEKT Suture Anchor MBI K143037…
Aevumed, Inc.2026—
*K143037SnapShot Fixation System
Summary page 5
…first) Product Code K260004 Aevumed PROTEKT Suture Anchor MBI K143037 SnapShot Fixation System JDR Device Descripti…
Biomet Manufacturing Corp20151

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K262809ArthroTAK Tendon Anchor KitArthroTAK, LLC20260

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 30 years and passes through 5 companies; a new generation was cleared every 2.2 years on median.
  • 3 of the 24 ancestors have a recall of any class.
  • Of its descendants, K262809 (ArthroTAK, LLC, 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All MBI devices

MBI Fastener, Fixation, Nondegradable, Soft Tissue: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · MBI

27in 2025

2007: 162008: 102009: 192010: 172011: 302012: 242013: 312014: 232015: 232016: 172017: 172018: 162019: 312020: 352021: 182022: 192023: 522024: 222025: 272026 (partial year): 30
2007high 52 (2023) · low 10 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MBI

58in 2025

2007: 80 days median2008: 69 days median2009: 82 days median2010: 76 days median2011: 75 days median2012: 94 days median2013: 100 days median2014: 101 days median2015: 85 days median2016: 94 days median2017: 70 days median2018: 91 days median2019: 90 days median2020: 83 days median2021: 107 days median2022: 64 days median2023: 57 days median2024: 30 days median2025: 58 days median2026 (partial year): 63 days median
2007high 107 (2021) · low 30 (2024)2026

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

Recalls per year · MBI

1in 2025

2007: 242008: 62009: 22010: 32011: 232012: 62013: 22017: 42018: 22020: 12023: 12024: 12025: 1
2007high 24 (2007) · low 0 (2014)2026

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

Adverse event reports per year · MBI

3,826in 2025

2007: 2402008: 3382009: 3552010: 2912011: 3282012: 3712013: 4422014: 5042015: 5072016: 7952017: 6752018: 1,0722019: 1,3032020: 1,4542021: 1,8902022: 1,5912023: 2,5032024: 3,7792025: 3,826
2007high 3,826 (2025) · low 240 (2007)2025

MAUDE reports naming product code MBI, 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
2007168024240
200810696338
200919822355
201017763291
2011307523328
201224946371
2013311002442
2014231010504
201523850507
201617940795
201717704675
2018169121,072
2019319001,303
2020358311,454
20211810701,890
2022196401,591
2023525712,503
2024223013,779
2025275813,826
202630630—

What is it indicated for?

The ArthroTAK Tendon Anchor Kit is intended to be used for soft-tissue to bone fixation in biceps tenodesis shoulder procedures.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K252635: ArthroTAK Tendon Anchor Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K252635

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Record history
  • FDA decision record loaded Oct 30, 2026
  • Summary read Oct 30, 2026 (extraction version 2d9447fa9ea4)
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026