510(k) Report

510(k) · Cleared

Cleared

Ace Stapler and Cartridge

K110829510(k) SpecialCleared Jun 3, 201171-day reviewClass II21 CFR 876.1500

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

Barosense, Inc. · OCW Endoscopic Tissue Approximation Device

Cleared on Jun 3, 2011 as substantially equivalent to K082044 (Barosense, Inc., 2010) after a 71-day review. Its family tree reaches back 7 generations to 1997. 1 later device descends from it.

Decided
Jun 3, 2011
Review
71 days
Class
Class II
Product code
OCW
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K972679 (1997). 15 ancestors in all, the oldest K934738 (1994). 1 later device descends from it, 1 citing it directly.

  1. Root · 7 generations backK972679 Endopath Endoscopic Tissue Fastening System (Etfs)Ethicon Endo-Surgery, Inc. · 1997
  2. 6 generations backK980022 Endopath Endoscopic Tissue Fastening System (Etfs)Ethicon Endo-Surgery, Inc. · 1998
  3. 5 generations backK994290 Bard Endoscopic Suturing SystemC.R. Bard, Inc. · 2000
  4. 4 generations backK062875 Endogastric Stomaphyx Device and AccessoriesEndogastric Solutions, Inc. · 2007
  5. 3 generations backK070151 Inscope Tissue Anchors, Knotting Elements and Tissue Anchor and…Ethicon Endo-Surgery, LLC · 2007
  6. 2 generations backK073671 Plicator GSX Suturing System, Plicator GSX, Plicator Instrument…Ndo Surgical, Inc. · 2008
  7. 1 generation backK082044 Ace Stapler, Model F0031Barosense, Inc. · 2010
  8. This deviceK110829 Ace Stapler and CartridgeBarosense, Inc. · 2011
  9. Descendant · cites it directly · 0 of its ownK120147 Ace Stapler and CartridgeBarosense, Inc. · 2012

Most influential descendants

Showing 1 of 1 · See all
  • K120147Ace Stapler and CartridgeBarosense, Inc. · 2012 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K972679Endopath Endoscopic Tissue Fastening System (Etfs)Ethicon Endo-Surgery, Inc.1997—
−6K980022Endopath Endoscopic Tissue Fastening System (Etfs)Ethicon Endo-Surgery, Inc.1998—
−5K994290Bard Endoscopic Suturing SystemC.R. Bard, Inc.2000—
−4K062875Endogastric Stomaphyx Device and AccessoriesEndogastric Solutions, Inc.2007—
−3K070151Inscope Tissue Anchors, Knotting Elements and Tissue Anchor and Knotting…Ethicon Endo-Surgery, LLC2007—
−2K073671Plicator GSX Suturing System, Plicator GSX, Plicator Instrument, Plicator GSX…Ndo Surgical, Inc.2008—
−1K082044Ace Stapler, Model F0031Barosense, Inc.2010—
0 (this device)K110829Ace Stapler and CartridgeBarosense, Inc.2011—
+1K120147Ace Stapler and CartridgeBarosense, Inc.2012—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
200120
200320
200610
200720

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
FIG. 1 — Lineage of K110829, 1997–2012Source: 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 OCW? 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 OCW device

  1. #1 K252400 Endomina EZFuse systemscore 12.1 · 5 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
*K082044Ace Stapler, Model F0031
Summary page 2
…Mnufcue Predicate device, 510(kf) BaroSense, Inc. ACE Stapler, model F0031 K082044 Redwood City, CA ACE Stapler Cartridge, model F0007 Device Description The ACETM Stapler is a surgical s…
Barosense, Inc.2010—

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K120147Ace Stapler and CartridgeBarosense, Inc.20120

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 6 companies; a new generation was cleared every 1.1 years on median.
  • 3 of the 15 ancestors have a recall of any class.
  • Of its descendants, K120147 (Barosense, Inc., 2012) has gone furthest, with 0 descendants of its own.

How does its category compare?

All OCW devices

OCW Endoscopic Tissue Approximation Device: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · OCW

1in 2025

2007: 52008: 42009: 32010: 42011: 12012: 12013: 22016: 22017: 22018: 22019: 12020: 12021: 32023: 32025: 12026 (partial year): 2
2007high 5 (2007) · low 0 (2014)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OCW

133in 2023

2007: 58 days median2008: 70 days median2009: 30 days median2010: 91 days median2021: 221 days median2023: 133 days median
2007high 221 (2021) · low 30 (2009)2026

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

Recalls per year · OCW

3so far in 2026, the most since 2007

2023: 12026 (partial year): 3
2007high 3 (2026) · low 0 (2007)2026

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

Adverse event reports per year · OCW

326in 2025

2007: 92008: 472009: 302010: 102011: 162012: 282013: 22014: 282015: 592016: 742017: 4202018: 4132019: 2912020: 1832021: 1982022: 2352023: 2272024: 2112025: 326
2007high 420 (2017) · low 2 (2013)2025

MAUDE reports naming product code OCW, 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
200755809
2008470047
2009330030
2010491010
20111—016
20121—028
20132—02
20140—028
20150—059
20162—074
20172—0420
20182—0413
20191—0291
20201—0183
202132210198
20220—0235
202331331227
20240—0211
20251—0326
20262—3—

What is it indicated for?

The BaroSense ACE Stapler and Cartridge are indicated for endoluminal trans-oral tissue approximation and ligation in the gastrointestinal tract.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K110829: Ace Stapler and Cartridge.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K110829

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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