510(k) Report

FDA product code · General and plastic surgery

Light Based Treatment For Cold Sores Herpes Simplex Virus-1

OKJClass II21 CFR 878.4860510(k) required4 decisions since 20120 recalls

4 FDA decisions since 2012. 510(k) reviews decided 2021–2025 took a median of 89 days (half between 82 and 111). No recall names this code. The most-cited predicate is K222205, named by 2 later devices.

Shortens time to healing of herpes simplex lesions on the lips, with time to healing defined as the time to patient described re-epithelialization.

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 OKJ 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 · OKJ

1in 2025

2012: 12022: 12024: 12025: 1
2007high 1 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OKJ

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

Recalls per year · OKJ

No recall names OKJ since 2007.

Adverse event reports per year · OKJ

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2025

MAUDE reports naming product code OKJ, 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—00
20121—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—01
20200—00
20210—00
20221—00
20230—00
20241—00
20251—00
20260—0—
FIG. 1 — OKJ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OKJ? 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