510(k) Report

FDA product code · Ear, nose and throat

Septal Stapler/Absorbable Staples

OLLClass II21 CFR 878.4750510(k) required1 decision since 20090 recalls

1 FDA decision since 2009. No recall names this code.

To approximate soft tissues by means of absorbable staples delivered via a pre-loaded stapler delivery system for use during nasal septal surgery, with or without cartilage reinserted. To connect internal nasal tissues to aid healing during nasal septum reconstruction.

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, ear, nose and throat panel

Twenty years of OLL 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 · OLL

1in 2009

2009: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OLL

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

Recalls per year · OLL

No recall names OLL since 2007.

Adverse event reports per year · OLL

2in 2025

2012: 12014: 72016: 12017: 22018: 62019: 22020: 12022: 22024: 12025: 2
2007high 7 (2014) · low 0 (2007)2025

MAUDE reports naming product code OLL, 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
20091—00
20100—00
20110—00
20120—01
20130—00
20140—07
20150—00
20160—01
20170—02
20180—06
20190—02
20200—01
20210—00
20220—02
20230—00
20240—01
20250—02
20260—0—
FIG. 1 — OLL by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OLL? 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 878.4750.