510(k) Report

FDA product code · General and plastic surgery

Suture, Nonabsorbable, Synthetic, Polyester

GASClass II21 CFR 878.5000510(k) required18 decisions since 19810 recalls

18 FDA decisions since 1981. No recall names this code. The most-cited predicate is K904436, named by 5 later devices.

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 GAS 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 · GAS

2in 2020

2010: 12020: 2
2007high 2 (2020) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GAS

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

Recalls per year · GAS

No recall names GAS since 2007.

Adverse event reports per year · GAS

3in 2025

2007: 352008: 472009: 562010: 242011: 252012: 732013: 212014: 122015: 12016: 22018: 32020: 12024: 12025: 3
2007high 73 (2012) · low 0 (2017)2025

MAUDE reports naming product code GAS, 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—035
20080—047
20090—056
20101—024
20110—025
20120—073
20130—021
20140—012
20150—01
20160—02
20170—00
20180—03
20190—00
20202—01
20210—00
20220—00
20230—00
20240—01
20250—03
20260—0—
FIG. 1 — GAS by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in GAS? 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 878.5000.