FDA product code · Ophthalmic

Projector, Ophthalmic

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

HOSClass I21 CFR 886.1680510(k) exempt9 decisions since 19780 recalls

FDA lists HOS as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 886.9 applies, such as a new intended use or a different fundamental technology. 9 FDA decisions since 1978. 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)

FIG. A — Illustration, ophthalmic panel

Twenty years of HOS 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 · HOS

FDA has decided no HOS device since 2007.

Median 510(k) review, days · HOS

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

Recalls per year · HOS

No recall names HOS since 2007.

Adverse event reports per year · HOS

No MAUDE report names HOS since 2007.

View these four charts as a table

Year	Median 510(k) review, days	MAUDE reports
2007	—	0
2008	—	0
2009	—	0
2010	—	0
2011	—	0
2012	—	0
2013	—	0
2014	—	0
2015	—	0
2016	—	0
2017	—	0
2018	—	0
2019	—	0
2020	—	0
2021	—	0
2022	—	0
2023	—	0
2024	—	0
2025	—	0
2026	—	—

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

Planning a device in HOS? 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

Projector, Ophthalmic

What has FDA decided in HOS lately?