FDA applicant

Morrison Center

Palm Florida, FL1 decision1994–19940 recalls

FDA records 1 decision for Morrison Center (Palm Florida, FL) in 1994: 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 Morrison Center’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Morrison Center since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Morrison”

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

Morrison Medical Products 8

Morrison Center

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Morrison”