FDA applicant

Storz Ophthalmics, Inc.

Clearwater4 decisions1981–19950 recalls

FDA records 4 decisions for Storz Ophthalmics, Inc. (Clearwater) from 1981 to 1995: 2 510(k) clearances and 2 original PMA approvals. Most are in product codes HQL (Intraocular Lens) and HQX (Implant, Orbital, Extra-Ocular). 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 Storz Ophthalmics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Storz Ophthalmics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Storz”

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

Storz Instrument Co. 101 Storz 6 Storz Medical AG 4 Storz AM Mark GmbH 2

Storz Ophthalmics, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Storz”