510(k) Report

FDA product code · Ear, nose and throat

Instrument, Ent Manual Surgical

LRCClass I21 CFR 874.4420510(k) exempt65 decisions since 19873 recalls

FDA lists LRC as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 874.9 applies, such as a new intended use or a different fundamental technology. 65 FDA decisions since 1987. 510(k) reviews decided 2021–2025 took a median of 135 days (half between 125 and 146). 3 recalls name this code, 0 of them Class I. The most-cited predicate is K102003, named by 7 later devices.

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, ear, nose and throat panel

Twenty years of LRC 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 · LRC

1in 2023

2008: 22009: 12010: 22011: 62012: 72013: 72014: 32015: 62016: 32017: 22018: 12019: 12020: 42022: 12023: 1
2007high 7 (2012) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LRC

131in 2020

2011: 106 days median2012: 50 days median2013: 104 days median2014: 29 days median2015: 105 days median2016: 100 days median2020: 131 days median
2007high 131 (2020) · low 29 (2014)2026

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

Recalls per year · LRC

1in 2024

2023: 12024: 1
2007high 1 (2023) · low 0 (2007)2026

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

Adverse event reports per year · LRC

44in 2025

2007: 12009: 82010: 112011: 142012: 482013: 532014: 532015: 412016: 392017: 322018: 422019: 192020: 202021: 232022: 252023: 142024: 512025: 44
2007high 53 (2013) · low 0 (2008)2025

MAUDE reports naming product code LRC, 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—01
20082—00
20091—08
20102—011
20116106014
2012750048
20137104053
2014329053
20156105041
20163100039
20172—032
20181—042
20191—019
20204131020
20210—023
20221—025
20231—114
20240—151
20250—044
20260—0—
FIG. 1 — LRC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LRC? 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 874.4420.