FDA product code

Medical device product code

Name: FDA decisions, review times, recalls and adverse event reports for product code LMX
Creator: 510(k) Report

LMX1 decision since 19810 recalls

1 FDA decision since 1981. No recall names this code. The most-cited predicate is P810007, named by 1 later device.

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)

Twenty years of LMX 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.

FIG. 1 — LMX by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in LMX? 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

Medical device product code

Which predicates do LMX devices cite most?

What has FDA decided in LMX lately?