510(k) Report

FDA product code · General and plastic surgery

Powered Laser Surgical Instrument With MicrobeamFractional Output

ONGClass II21 CFR 878.4810510(k) required35 decisions since 20093 recalls

35 FDA decisions since 2009. 510(k) reviews decided 2021–2025 took a median of 148 days (half between 93 and 202). 3 recalls name this code, 0 of them Class I. The most-cited predicate is K130028, named by 4 later devices.

A LASER (Light Amplification by Stimulated Emission of Radiation) based device having coherence, collimated and typically monochromatic radiation. The laser output is in form of tiny beams in micro range. Typically, indicated to be used in medical specialties of general and plastic surgery and of dermatology/aesthetic to destroy, remove or coagulate tissue, generally soft tissue. Indication for Use can be general…

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 ONG 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 · ONG

4in 2025

2009: 42010: 42011: 62012: 22013: 32014: 22017: 12018: 22020: 12021: 12022: 32023: 12024: 12025: 4
2007high 6 (2011) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ONG

97in 2025

2009: 160 days median2010: 176 days median2011: 122 days median2013: 243 days median2022: 203 days median2025: 97 days median
2007high 243 (2013) · low 97 (2025)2026

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

Recalls per year · ONG

2in 2024

2010: 12024: 2
2007high 2 (2024) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · ONG

1in 2025

2010: 32011: 22012: 42013: 42014: 62015: 82016: 82017: 402018: 272019: 152020: 32021: 92022: 22023: 32024: 112025: 1
2007high 40 (2017) · low 0 (2007)2025

MAUDE reports naming product code ONG, 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
2009416000
2010417613
2011612202
20122—04
2013324304
20142—06
20150—08
20160—08
20171—040
20182—027
20190—015
20201—03
20211—09
2022320302
20231—03
20241—211
202549701
20260—0—
FIG. 1 — ONG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ONG? 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 878.4810.