FDA product code

Medical device product code

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

PBL1 decision since 20120 recalls

1 FDA decision since 2012. No recall names this code.

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

Planning a device in PBL? 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 PBL devices have the deepest lineage?

What has FDA decided in PBL lately?