510(k) Report

510(k) · Cleared

Cleared

DynaClipTM Bone Staple

K181781510(k) TraditionalCleared Nov 5, 2018125-day reviewClass II21 CFR 888.3030

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

MedShape, Inc. · JDR Staple, Fixation, Bone

Cleared on Nov 5, 2018 as substantially equivalent to K124045 (Solana Surgical, LLC, 2013) after a 125-day review. Its family tree reaches back 4 generations to 1990. 2 later devices descend from it.

Decided
Nov 5, 2018
Review
125 days
Class
Class II
Product code
JDR
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K902307 (1990). 5 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by generationDescendants, by generation 3 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant K124045 · Fuseforce Implant System · Solana Surgical, LLC · 2013K070031 · Memometal Memory Staples · Memometal Technologies · 2007K993714 · Memograph Staple, Warm System · Biomedical Ent., Inc. · 2000K902307 · Shaw II Hemostatic Surgery System · Hemostatic Surgery Corp. · 1990 · recalled0
  1. Root · 4 generations backK902307 Shaw II Hemostatic Surgery SystemHemostatic Surgery Corp. · 1990 · Recalled
  2. 3 generations backK993714 Memograph Staple, Warm SystemBiomedical Ent., Inc. · 2000
  3. 2 generations backK070031 Memometal Memory StaplesMemometal Technologies · 2007
  4. 1 generation backK124045 Fuseforce Implant SystemSolana Surgical, LLC · 2013
  5. This deviceK181781 DynaClipTM Bone StapleMedShape, Inc. · 2018
  6. Descendant · cites it directly · 1 of its ownK254110 DynaNail Mini; DynaNail Hybrid; DynaNail Helix; DynaClip; DynaClip…MedShape, Inc. · 2026
  7. Descendant · 2 generations on · 0 of its ownK260995 DynaNail Helix® Fixation SystemMedShape, Inc. · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K254110DynaNail Mini; DynaNail Hybrid; DynaNail Helix; DynaClip; DynaClip Forte; DynaClip…MedShape, Inc. · 2026 · cites it directly1descendant
  • K260995DynaNail Helix® Fixation SystemMedShape, Inc. · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K902307Shaw II Hemostatic Surgery SystemHemostatic Surgery Corp.19902
−3K993714Memograph Staple, Warm SystemBiomedical Ent., Inc.2000—
−2K070031Memometal Memory StaplesMemometal Technologies2007—
−1K124045Fuseforce Implant SystemSolana Surgical, LLC2013—
0 (this device)K181781DynaClipTM Bone StapleMedShape, Inc.2018—
+1K254110DynaNail Mini; DynaNail Hybrid; DynaNail Helix; DynaClip; DynaClip Forte…MedShape, Inc.2026—
+2K260995DynaNail Helix® Fixation SystemMedShape, Inc.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202620
FIG. 1 — Lineage of K181781, 1990–2026Source: 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 JDR? 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 JDR device

  1. #1 K243658 TMC Compression Implant Systemscore 16.7 · 18 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? (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
*K124045Fuseforce Implant System
Summary page 4
…JDR, 21 CFR 888.3030 Class II E. Predicate Device: Solana Surgical, LLC (now Wright Medical), FuseForce® Implant, K124045 F. Physical Description: The proposed MedShape DynaClip Bone Staple is a sterile, single use orthopedic…
Solana Surgical, LLC2013—

Also cleared against K124045: 5 other devices →

What descends from it? (2)

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

NumberDeviceApplicantDecidedDescendants
K254110DynaNail Mini; DynaNail Hybrid; DynaNail Helix; DynaClip; DynaClip Forte; DynaClip…MedShape, Inc.20261

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 28 years and passes through 5 companies; a new generation was cleared every 7.1 years on median.
  • 1 of the 5 ancestors has a recall of any class.
  • Of its descendants, K254110 (MedShape, Inc., 2026) has gone furthest, with 1 descendant of its own.
  • 5 other devices also cite its predicate K124045.

How does its category compare?

All JDR devices

JDR Staple, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · JDR

3in 2025

2007: 82008: 52010: 22011: 12012: 12013: 92014: 112015: 72016: 62017: 92018: 82019: 52020: 42021: 32022: 52023: 92024: 42025: 32026 (partial year): 2
2007high 11 (2014) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JDR

65in 2025

2007: 70 days median2008: 89 days median2013: 137 days median2014: 97 days median2015: 111 days median2016: 101 days median2017: 172 days median2018: 107 days median2019: 149 days median2020: 161 days median2021: 62 days median2022: 107 days median2023: 72 days median2024: 29 days median2025: 65 days median
2007high 172 (2017) · low 29 (2024)2026

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

Recalls per year · JDR

11in 2022

2008: 12015: 12018: 12020: 12022: 112026 (partial year): 2
2007high 11 (2022) · low 0 (2007)2026

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

Adverse event reports per year · JDR

314in 2025

2007: 32008: 142009: 102010: 352011: 622012: 342013: 272014: 492015: 482016: 762017: 1162018: 2392019: 2422020: 2342021: 2102022: 2022023: 1752024: 2062025: 314
2007high 314 (2025) · low 3 (2007)2025

MAUDE reports naming product code JDR, 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
200787003
2008589114
20090—010
20102—035
20111—062
20121—034
20139137027
20141197049
20157111148
20166101076
201791720116
201881071239
201951490242
202041611234
20213620210
2022510711202
20239720175
20244290206
20253650314
20262—2—

What is it indicated for?

The MedShape DynaClip™ Bone Staple is intended to be used for fracture and osteotomy fixation and joint arthrodesis of the hand and foot.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K181781: DynaClipTM Bone Staple.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K181781

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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