510(k) Report

FDA product code · General and plastic surgery

Stapler, Surgical

GAGClass II21 CFR 878.4740510(k) required43 decisions since 19765 recalls

43 FDA decisions since 1976. 510(k) reviews decided 2021–2025 took a median of 114 days (half between 65 and 141). 5 recalls name this code, 0 of them Class I. The most-cited predicate is K892927, named by 4 later devices.

A surgical stapler for internal use is a specialized prescription device used to deliver compatible staples to internal tissues during surgery for resection, transection, and creating anastomoses.

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

FIG. A — Illustration, general and plastic surgery panel

Twenty years of GAG at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · GAG

2in 2025

2022: 12023: 42024: 32025: 22026 (partial year): 1
2007high 4 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAG

138in 2024

2023: 102 days median2024: 138 days median
2007high 138 (2024) · low 102 (2023)2026

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

Recalls per year · GAG

1in 2018

2010: 12012: 12018: 1
2007high 1 (2010) · low 0 (2007)2026

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

Adverse event reports per year · GAG

1,065in 2025

2007: 9192008: 3662009: 182010: 222011: 192012: 492013: 1352014: 3022015: 1442016: 752017: 962018: 812019: 702020: 472021: 532022: 502023: 1092024: 1,1262025: 1,065
2007high 1,126 (2024) · low 18 (2009)2025

MAUDE reports naming product code GAG, 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—0919
20080—0366
20090—018
20100—122
20110—019
20120—149
20130—0135
20140—0302
20150—0144
20160—075
20170—096
20180—181
20190—070
20200—047
20210—053
20221—050
202341020109
2024313801,126
20252—01,065
20261—0—
FIG. 1 — GAG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in GAG? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 878.4740.