FDA applicant

Automated Lens System

Miami, FL1 decision1988–19880 recalls

FDA records 1 decision for Automated Lens System (Miami, FL) in 1988: 1 510(k) clearance. All are in product code HQG (Lens, Spectacle, Non-Custom (Prescription)). 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 Automated Lens System’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automated Lens System since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Automated”

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

Automated Medical Products Corp. 6 Automated Screening Devices 2 Automated IV Systems, Inc. 1 Automated Ophthalmics, Inc. 1 Automated Testing Services, Ltd. 1 Automated Imaging Diagnostics, LLC 1

Automated Lens System

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Automated”