510(k) Report

510(k) · Cleared

Cleared

Magseed Magnetic Marker System

K163541510(k) SpecialCleared Jan 13, 201728-day reviewClass II21 CFR 878.4300

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

Endomagnetics Ltd., · PBY Temporary Tissue Marker

Cleared on Jan 13, 2017 as substantially equivalent to K153044 (Endomagnetics Ltd.,, 2016) after a 28-day review. Its family tree reaches back 8 generations to 2003. 12 later devices descend from it.

Decided
Jan 13, 2017
Review
28 days
Class
Class II
Product code
PBY
Recalls
None
Predicates
1

Its longest line of descent runs back 8 generations to K023694 (2003). 22 ancestors in all, the oldest K970817 (1997). 12 later devices descend from it, 4 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2011: 2 other ancestors2010: 2 other ancestors2008: 1 other ancestor2007: 1 other ancestor2004: 2 other ancestors1997: 1 other ancestor2002: 2 other ancestors2001: 1 other ancestor2000: 2 other ancestors2023: 4 descendants cleared2018: 1 descendant cleared2021: 2 descendants cleared2024: 3 descendants cleared2022: 1 descendant cleared2025: 1 descendant clearedK023694 · Bio-Mark Resorbable Biopsy Site Marker and Bio-Mark Permanent Biopsy Site Marker · Biopsy Sciences, LLC · 2003K051421 · Inter V Brand V-Mark Breast Biopsy Site Marker with Titanium Anchor · Medical Device Technologies, Inc. · 2005K053518 · Interv Brand V-Mark Breast Biopsy Site Marker with Titanium Anchor · Medical Device Technologies, Inc. · 2006K060769 · Hydromark Biopsy Site Marker · Biopsy Sciences, LLC · 2006×2: 2 generations cleared close together, K083006 (2009), K090501 (2009) K120804 · Cianna Medical Tissue Marker and Delivery System · Cianna Medical · 2013K153044 · Sentimag System, Sentimark Magnetic Marker Systerm · Endomagnetics Ltd., · 20161995200020052010201520202025
  1. Root · 8 generations backK023694 Bio-Mark Resorbable Biopsy Site Marker and Bio-Mark Permanent Biopsy…Biopsy Sciences, LLC · 2003
  2. 7 generations backK051421 Inter V Brand V-Mark Breast Biopsy Site Marker with Titanium AnchorMedical Device Technologies, Inc. · 2005
  3. 6 generations backK053518 Interv Brand V-Mark Breast Biopsy Site Marker with Titanium AnchorMedical Device Technologies, Inc. · 2006
  4. 5 generations backK060769 Hydromark Biopsy Site MarkerBiopsy Sciences, LLC · 2006
  5. 4 generations backK083006 Biopsy Sciences, Inc., Hydromark Breast Biopsy Site MarkerBiopsy Sciences, LLC · 2009
  6. 3 generations backK090501 Biopsy Sciences Hydromark Breast Biopsy Site Marker, Models…Biopsy Sciences, LLC · 2009
  7. 2 generations backK120804 Cianna Medical Tissue Marker and Delivery SystemCianna Medical · 2013
  8. 1 generation backK153044 Sentimag System, Sentimark Magnetic Marker SystermEndomagnetics Ltd., · 2016
  9. This deviceK163541 Magseed Magnetic Marker SystemEndomagnetics Ltd., · 2017
  10. Descendant · cites it directly · 5 of its ownK210600 MOLLIMolli Surgical, Inc. · 2021
  11. Descendant · 2 generations on · 4 of its ownK223107 MOLLI 2Molli Surgical, Inc. · 2023
  12. Descendant · 3 generations on · 3 of its ownK231579 MOLLI 2Molli Surgical, Inc. · 2023 · Recalled
  13. Descendant · cites it directly · 2 of its ownK200734 Sirius Pintuition Seed, Sirius Pintuition Probe, Sirius Pintuition…Sirius Medical Systems B.V. · 2021
  14. Descendant · cites it directly · 2 of its ownK173587 Magseed Magnetic Marker SysttemEndomagnetics Ltd., · 2018

Showing 5 of 12 descendants. See all descendants

Descendants cleared per year

2018: 12021: 22022: 12023: 42024: 32025: 1
2018high 4 (2023) · low 0 (2019)2026

Most influential descendants

Showing 5 of 12 · See all
  • K210600MOLLIMolli Surgical, Inc. · 2021 · cites it directly5descendants
  • K223107MOLLI 2Molli Surgical, Inc. · 2023 · 2 generations on4descendants
  • K231579MOLLI 2Molli Surgical, Inc. · 2023 · 3 generations on3descendants
  • K200734Sirius Pintuition Seed, Sirius Pintuition Probe, Sirius Pintuition Base UnitSirius Medical Systems B.V. · 2021 · cites it directly2descendants
  • K173587Magseed Magnetic Marker SysttemEndomagnetics Ltd., · 2018 · cites it directly2descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−8K023694Bio-Mark Resorbable Biopsy Site Marker and Bio-Mark Permanent Biopsy Site MarkerBiopsy Sciences, LLC2003—
−7K051421Inter V Brand V-Mark Breast Biopsy Site Marker with Titanium AnchorMedical Device Technologies, Inc.2005—
−6K053518Interv Brand V-Mark Breast Biopsy Site Marker with Titanium AnchorMedical Device Technologies, Inc.2006—
−5K060769Hydromark Biopsy Site MarkerBiopsy Sciences, LLC2006—
−4K083006Biopsy Sciences, Inc., Hydromark Breast Biopsy Site MarkerBiopsy Sciences, LLC2009—
−3K090501Biopsy Sciences Hydromark Breast Biopsy Site Marker, Models 4005-02-15-T1…Biopsy Sciences, LLC2009—
−2K120804Cianna Medical Tissue Marker and Delivery SystemCianna Medical2013—
−1K153044Sentimag System, Sentimark Magnetic Marker SystermEndomagnetics Ltd.,2016—
0 (this device)K163541Magseed Magnetic Marker SystemEndomagnetics Ltd.,2017—
+1K210600MOLLIMolli Surgical, Inc.2021—
+2K223107MOLLI 2Molli Surgical, Inc.2023—
+3K231579MOLLI 2Molli Surgical, Inc.20231
+1K200734Sirius Pintuition Seed, Sirius Pintuition Probe, Sirius Pintuition Base UnitSirius Medical Systems B.V.2021—
+1K173587Magseed Magnetic Marker SysttemEndomagnetics Ltd.,2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199710
200020
200110
200220
200420
200710
200810
201020
201120

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201810
202120
202210
202340
202430
202510
FIG. 1 — Lineage of K163541, 2003–2025Source: 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 PBY? 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 PBY device

  1. #1 K222643 Sirius Pintuition Seed, Sirius Pintuition…score 9.9 · 10 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
*K153044Sentimag System, Sentimark Magnetic Marker Systerm
Summary page 5
…21 CFR 878.4300 Device Classification: Class II Product Code: PBY 1.3 PREDICATE DEVICE Sentimag System, Sentimark Magnetic Marker System (K153044). 1.4 DESCRIPTION OF DEVICE The Magseed Magnetic Marker is identical to the Sentimark Magentic marker described in K153044.…
Endomagnetics Ltd.,2016—

Also cleared against K153044: 2 other devices →

What descends from it? (12)

See all 12

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

NumberDeviceApplicantDecidedDescendants
K210600MOLLIMolli Surgical, Inc.20215
K200734Sirius Pintuition Seed, Sirius Pintuition Probe, Sirius Pintuition Base UnitSirius Medical Systems B.V.20212
K173587Magseed Magnetic Marker SysttemEndomagnetics Ltd.,20182
K222832Sentimag SystemEndomagnetics Ltd.,20230

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 14 years and passes through 4 companies; a new generation was cleared every 2.5 years on median.
  • 3 of the 22 ancestors have a recall of any class.
  • Of its descendants, K210600 (Molli Surgical, Inc., 2021) has gone furthest, with 5 descendants of its own.
  • 2 other devices also cite its predicate K153044.

How does its category compare?

All PBY devices

PBY Temporary Tissue Marker: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · PBY

1in 2023

2013: 12016: 12017: 22021: 12022: 12023: 1
2007high 2 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PBY

Too few PBY 510(k)s in any year since 2007 to give a median.

Recalls per year · PBY

No recall names PBY since 2007.

Adverse event reports per year · PBY

1in 2024

2017: 12019: 12023: 12024: 1
2007high 1 (2017) · low 0 (2007)2025

MAUDE reports naming product code PBY, 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—00
20080—00
20090—00
20100—00
20110—00
20120—00
20131—00
20140—00
20150—00
20161—00
20172—01
20180—00
20190—01
20200—00
20211—00
20221—00
20231—01
20240—01
20250—00
20260—0—

What is it indicated for?

The Endomag Magseed Magnetic Marker is intended to be placed percutaneously in the breast to mark temporarily (< 30 days) a lumpectomy site intended for surgical removal. Using imaging guidance (such as ultrasound or radiography) or aided by non-imaging guidance (Endomag Sentimag® System) the Endomag Magseed Magnetic Marker is located and surgically removed with the target tissue.

The Endomag Sentimag® System is intended for the non-imaging detection and localization of the "Endomag Magseed Magnetic Marker" that has been implanted in a lumpectomy site intended for surgical removal.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K163541: Magseed Magnetic Marker System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K163541

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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