FDA applicant

Inno-Lite Co., Inc.

Duluth, GA1 decision1990–19900 recalls

FDA records 1 decision for Inno-Lite Co., Inc. (Duluth, GA) in 1990: 1 510(k) clearance. All are in product code HQZ (Frame, Spectacle). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, ophthalmic panel, where it files most

How often FDA has decided Inno-Lite Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Inno-Lite Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Inno-Lite Co., Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Inno-Lite Co., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Inno-Lite”

FDA records each applicant name separately; these may or may not be the same firm.

Inno-Health Technology, Inc. 2 Inno Lifecare 1 INNO Holdings Inc. DBA Innovasis 1

Inno-Lite Co., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Inno-Lite”