FDA product code · Ophthalmic

Guide And Positioner, Ophthalmic Drug Delivery Device

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

QQQClass I21 CFR 886.4300Pathway set case by case0 decisions0 recalls

0 FDA decisions. No recall names this code.

To provide a guide and/or positioner for filling of a drug delivery 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)

FIG. A — Illustration, ophthalmic panel

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

Planning a device in QQQ? 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

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