510(k) Report

FDA product code · Ophthalmic

Lacrimal Stents And Intubation Sets

OKSClass U510(k) required31 decisions since 19880 recalls

31 FDA decisions since 1988. 510(k) reviews decided 2021–2025 took a median of 246 days (half between 246 and 246). No recall names this code. The most-cited predicate is K061404, named by 3 later devices.

Lacrimal stents and intubations sets are intended to repair the lacrimal drainage system. Lacrimal stents and intubations sets are indicated for, but limited to, the treatment of epiphora in infants and adults; canalicular pathologies such as stenosis; obstruction or laceration; and conditions requiring dacryocystorhinostomy (conventional or laser); or imperforation of the nasolacrimal duct in an infant.

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, ophthalmic panel

Twenty years of OKS 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 · OKS

1in 2021

2012: 72013: 22014: 12015: 12016: 22017: 12020: 12021: 1
2007high 7 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OKS

277in 2012

2012: 277 days median
2007high 277 (2012)2026

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

Recalls per year · OKS

No recall names OKS since 2007.

Adverse event reports per year · OKS

3in 2022

2011: 22012: 32013: 32014: 82015: 142016: 212017: 182018: 62019: 82020: 22021: 62022: 3
2007high 21 (2016) · low 0 (2007)2025

MAUDE reports naming product code OKS, 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
20090—00
20100—00
20110—02
2012727703
20132—03
20141—08
20151—014
20162—021
20171—018
20180—06
20190—08
20201—02
20211—06
20220—03
20230—00
20240—00
20250—00
20260—0—
FIG. 1 — OKS by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OKS? 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