510(k) Report

510(k) · Cleared

Cleared

Tigon Medical Knotless and Dual Javelin All-Suture Anchors

K252596510(k) TraditionalCleared Dec 4, 2025111-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

Tigon Medical · MBI Fastener, Fixation, Nondegradable, Soft Tissue

Cleared on Dec 4, 2025 as substantially equivalent to K242529 (Tigon Medical, 2024) and 1 other predicate after a 111-day review. Its family tree reaches back 10 generations to 1996. 1 later device descends from it.

Decided
Dec 4, 2025
Review
111 days
Class
Class II
Product code
MBI
Recalls
None
Predicates
2

Its longest line of descent runs back 10 generations to K961555 (1996). 50 ancestors in all, the oldest K813581 (1982). 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2013: 1 other ancestor2012: 2 other ancestors2011: 1 other ancestor2004: 3 other ancestors2007: 4 other ancestors2002: 1 other ancestor2001: 7 other ancestors2000: 6 other ancestors1999: 1 other ancestor1997: 3 other ancestors1982: 1 other ancestor2005: 2 other ancestors1998: 1 other ancestor1996: 2 other ancestors1993: 1 other ancestor2006: 1 other ancestor1995: 1 other ancestor1994: 1 other ancestor1990: 1 other ancestor2026: 1 descendant clearedReference device: K230311 · HyperSuture · Threadstone, LLC · 2023Reference device: K220464 · Tigon Medical Gryphon Anchor Line · Tigon Medical · 2023Reference device: K182507 · Tigon Medical Tissue Anchors · Tigon Medical · 2019K961555 · Acufex Tag Bioabsorbable Anchors · Acufex Microsurgical, Inc. · 1996K031685 · Tag Rod Bioraptor Suture Anchor 7209317, 7209318 · Smith & Nephew, Inc. · 2003 · recalledK053344 · Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture Anchor · Smith & Nephew, Inc. · 2006K061863 · Arthrex Corkscrew Suture Anchor, Tak, and Pushlock Family · Arthrex, Inc. · 2006K071177 · Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite Tak, Bio-Composite Corkscrew · Arthrex, Inc. · 2007K082810 · Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock, Bio-Composite Tak and Bio-Composite Corkscrew · Arthrex, Inc. · 2009×2: 2 generations cleared close together, K101823 (2011), K110545 (2011) K133671 · Iconix All Suture Anchors · Stryker Corp. · 2014K242529 · Tigon Medical All-Suture Anchors (ASA) · Tigon Medical · 202419801990200020102020
  1. Root · 10 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 6 generations between
  3. 3 generations backK110545 Smith & Nephew Next Generation Fully Threaded Peek Suture Anchor…Smith & Nephew, Inc. · 2011
  4. 2 generations backK133671 Iconix All Suture AnchorsStryker Corp. · 2014
  5. 1 generation backK242529 Tigon Medical All-Suture Anchors (ASA)Tigon Medical · 2024
  6. This deviceK252596 Tigon Medical Knotless and Dual Javelin All-Suture AnchorsTigon Medical · 2025
  7. Descendant · cites it directly · 0 of its ownK260921 Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture…Tigon Medical · 2026
Show all 10 generations
  1. Root · 10 generations backK961555 Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc. · 1996
  2. 9 generations backK031685 Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc. · 2003 · Recalled
  3. 8 generations backK053344 Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5…Smith & Nephew, Inc. · 2006
  4. 7 generations backK061863 Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc. · 2006
  5. 6 generations backK071177 Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock…Arthrex, Inc. · 2007
  6. 5 generations backK082810 Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite…Arthrex, Inc. · 2009
  7. 4 generations backK101823 Arthrex Swivelock AnchorsArthrex, Inc. · 2011 · Recalled
  8. 3 generations backK110545 Smith & Nephew Next Generation Fully Threaded Peek Suture Anchor…Smith & Nephew, Inc. · 2011
  9. 2 generations backK133671 Iconix All Suture AnchorsStryker Corp. · 2014
  10. 1 generation backK242529 Tigon Medical All-Suture Anchors (ASA)Tigon Medical · 2024
  11. This deviceK252596 Tigon Medical Knotless and Dual Javelin All-Suture AnchorsTigon Medical · 2025

Most influential descendants

Showing 1 of 1 · See all
  • K260921Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor LineTigon Medical · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−10K961555Acufex Tag Bioabsorbable AnchorsAcufex Microsurgical, Inc.1996—
−9K031685Tag Rod Bioraptor Suture Anchor 7209317, 7209318Smith & Nephew, Inc.20035
−8K053344Bioraptor Suture Anchor, Twinfix 2.8 MM Suture Anchor, Twinfix 3.5 MM Suture…Smith & Nephew, Inc.2006—
−7K061863Arthrex Corkscrew Suture Anchor, Tak, and Pushlock FamilyArthrex, Inc.2006—
−6K071177Arthrex Bio- Composite Suture Anchors: Bio-Composite Pushlock, Bio-Composite…Arthrex, Inc.2007—
−5K082810Arthrex Bio-Composite Suture Anchors: Arthrex Bio-Composite Pushlock…Arthrex, Inc.2009—
−4K101823Arthrex Swivelock AnchorsArthrex, Inc.20116
−3K110545Smith & Nephew Next Generation Fully Threaded Peek Suture Anchor (Ngftsa PK)Smith & Nephew, Inc.2011—
−2K133671Iconix All Suture AnchorsStryker Corp.2014—
−1K242529Tigon Medical All-Suture Anchors (ASA)Tigon Medical2024—
0 (this device)K252596Tigon Medical Knotless and Dual Javelin All-Suture AnchorsTigon Medical2025—
+1K260921Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor LineTigon Medical2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198210
199010
199310
199410
199510
199620
199730
199810
199910
200060
200170
200210
200430
200520
200610
200740
201110
201220
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K252596, 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
*K242529Tigon Medical All-Suture Anchors (ASA)
Summary page 4
…? The Tigon Medical Knotless and Dual Javelin All-Suture Anchors are an extension to the Tigon Medical All­ Suture Anchor line cleared in K242529 (December 20, 2024 ). The Tigon Medical Javelin All-Suture Anchors are intended for the reattachment of soft tissue to bone for t…
Tigon Medical2024—
*K130458Knotless Fibertak Suture Anchor
Summary page 5
…nel: MBI Predicate Devices: Tigon Medical All-Suture Anchors (K242529) [Primary Predicate] Arthrex Knotless FiberTak Suture Anchor (K130458) Reference: Threadstone HyperSuture (K230311) Reference: Tigon Medical Toma…
Arthrex, Inc.2013—
†K230311HyperSutureThreadstone, LLC2023—
†K220464Tigon Medical Gryphon Anchor LineTigon Medical2023—
†K182507Tigon Medical Tissue AnchorsTigon Medical2019—

Also cleared against K242529: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K260921Tigon Medical Static Javelin All-Suture Anchors & Javelin All-Suture Anchor LineTigon Medical20260

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 2.0 years on median.
  • 6 of the 50 ancestors have a recall of any class.
  • Of its descendants, K260921 (Tigon Medical, 2026) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K242529.

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. 2025, 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 Tigon Medical Knotless and Dual Javelin All-Suture Anchors are an extension to the Tigon Medical All-Suture Anchor line cleared in K242529 (December 20, 2024). The Tigon Medical Javelin All-Suture Anchors are intended for the reattachment of soft tissue to bone for the following indications: • Elbow: Biceps Tendon Reattachment. Ulnar or Radial Collateral Ligament Reconstruction • Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair…

Read the full statement (159 words)

The Tigon Medical Knotless and Dual Javelin All-Suture Anchors are an extension to the Tigon Medical All-Suture Anchor line cleared in K242529 (December 20, 2024). The Tigon Medical Javelin All-Suture Anchors are intended for the reattachment of soft tissue to bone for the following indications:

• Elbow: Biceps Tendon Reattachment. Ulnar or Radial Collateral Ligament Reconstruction

• Shoulder: Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromio-Clavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Repair

• Hand/Wrist: Scaphulolunate Ligament Reconstruction, Carpal Ligament Reconstruction, Repair/Reconstruction of Collateral Ligaments, Repair of Flexor and Extensor Tendons at the PIP, DIP and MCP Joints for all Digits, Digital Tendon Repair

• Foot/Ankle: Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair, Metatarsal Ligament Repair, Hallux Valgus Reconstruction, Digital Tendon Transfers, Mid-foot Reconstruction

• Knee: Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Patellar Tendon Repair, Posterior Oblique Ligament Repair, Iliotibial Band Tenodesis

• Hip: Capsular Repair, Acetabular Labral Repair, Gluteal Tendon Repair

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K252596: Tigon Medical Knotless and Dual Javelin All-Suture Anchors.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K252596

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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