510(k) Report

FDA product code · Gastroenterology and urology

Lipoprotein, Low Density, Removal

MMYClass IIIPMA required2 decisions since 19962 recalls

2 FDA decisions since 1996. 2 recalls name this code, 0 of them Class I.

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, gastroenterology and urology panel

Twenty years of MMY 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 · MMY

3in 2025

2007: 12009: 32010: 22012: 32013: 12015: 52016: 72017: 32018: 32019: 42020: 22021: 32022: 32023: 12024: 22025: 32026 (partial year): 2
2007high 7 (2016) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MMY

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

Recalls per year · MMY

1in 2022

2022: 1
2007high 1 (2022) · low 0 (2007)2026

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

Adverse event reports per year · MMY

2in 2025

2012: 12013: 12014: 62015: 12016: 52017: 22018: 42019: 22020: 22022: 12025: 2
2007high 6 (2014) · low 0 (2007)2025

MAUDE reports naming product code MMY, 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
20071—00
20080—00
20093—00
20102—00
20110—00
20123—01
20131—01
20140—06
20155—01
20167—05
20173—02
20183—04
20194—02
20202—02
20213—00
20223—11
20231—00
20242—00
20253—02
20262—0—
FIG. 1 — MMY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MMY? 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