510(k) Report

FDA product code · General and plastic surgery

Polymer, Composite Synthetic Ptfe With Carbon-Fiber, Ent

ESFClass II21 CFR 878.3500510(k) required2 decisions since 19820 recalls

2 FDA decisions since 1982. No recall names this code.

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 ESF 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 · ESF

FDA has decided no ESF device since 2007.

Median 510(k) review, days · ESF

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

Recalls per year · ESF

No recall names ESF since 2007.

Adverse event reports per year · ESF

No MAUDE report names ESF since 2007.

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
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — ESF by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

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

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Related product codes

Other codes under 21 CFR 878.3500.