510(k) Report

FDA product code · General and plastic surgery

Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

ONFClass II21 CFR 878.4810510(k) required74 decisions since 20080 recalls

74 FDA decisions since 2008. 510(k) reviews decided 2021–2025 took a median of 121 days (half between 86 and 197). No recall names this code. The most-cited predicate is K122995, named by 7 later devices.

A light based non-laser device that provides thermal effect including broad spectrum source devices such as intense pulse light (ipl). Typically, indicated to be used in medical specialties of general and plastic surgery and of dermatology/aesthetic. Indication for use can be general and/or specific.The classification regulation 21 cfr 878.4810 describes a device that is carbon dioxide or argon laser intended to…

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 ONF 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 · ONF

4in 2025

2008: 12009: 52010: 42011: 52012: 32013: 102014: 72015: 32016: 52018: 22019: 22020: 42021: 42022: 42023: 52024: 52025: 42026 (partial year): 1
2007high 10 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ONF

192in 2025

2009: 160 days median2010: 137 days median2011: 166 days median2012: 134 days median2013: 113 days median2014: 118 days median2015: 111 days median2016: 87 days median2020: 104 days median2021: 101 days median2022: 165 days median2023: 86 days median2024: 168 days median2025: 192 days median
2007high 192 (2025) · low 86 (2023)2026

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

Recalls per year · ONF

No recall names ONF since 2007.

Adverse event reports per year · ONF

5in 2025

2014: 22015: 42016: 62017: 12018: 12019: 22020: 12021: 22022: 22023: 22024: 32025: 5
2007high 6 (2016) · low 0 (2007)2025

MAUDE reports naming product code ONF, 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
20081—00
2009516000
2010413700
2011516600
2012313400
20131011300
2014711802
2015311104
201658706
20170—01
20182—01
20192—02
2020410401
2021410102
2022416502
202358602
2024516803
2025419205
20261—0—
FIG. 1 — ONF by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ONF? 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 878.4810.