510(k) Report

FDA product code · General and plastic surgery

Single-Use Reprocessed Ultrasonic Surgical Instruments

NLQClass U510(k) required27 decisions since 20013 recalls

27 FDA decisions since 2001. 510(k) reviews decided 2021–2025 took a median of 130 days (half between 96 and 155). 3 recalls name this code, 0 of them Class I. The most-cited predicate is K202554, named by 1 later device.

Single-use reprocessed versions of the ultrasonic devices used in surgical procedures either for fragmentation, emulsification and aspiration of soft tissue and hard tissue or for ligation of vessels (under product code “LFL”). Reprocessing validation data for this device type must be included in a 510(k) submission.. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).

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 NLQ 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 · NLQ

1in 2025

2009: 12010: 22012: 12014: 32015: 22016: 12017: 32018: 12019: 22020: 12021: 12024: 22025: 1
2007high 3 (2014) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · NLQ

94in 2017

2014: 303 days median2017: 94 days median
2007high 303 (2014) · low 94 (2017)2026

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

Recalls per year · NLQ

1in 2025

2008: 12023: 12025: 1
2007high 1 (2008) · low 0 (2007)2026

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

Adverse event reports per year · NLQ

44in 2025

2007: 172008: 252009: 122010: 332011: 582012: 1132013: 1112014: 632015: 932016: 722017: 872018: 562019: 452020: 282021: 402022: 312023: 162024: 192025: 44
2007high 113 (2012) · low 12 (2009)2025

MAUDE reports naming product code NLQ, 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—017
20080—125
20091—012
20102—033
20110—058
20121—0113
20130—0111
20143303063
20152—093
20161—072
2017394087
20181—056
20192—045
20201—028
20211—040
20220—031
20230—116
20242—019
20251—144
20260—0—
FIG. 1 — NLQ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NLQ? 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