FDA applicant

Carl Zeiss Meditec Cataract Technologies

Reno, NV1 decision2026–20260 recalls

FDA records 1 decision for Carl Zeiss Meditec Cataract Technologies (Reno, NV) in 2026: 1 510(k) clearance. All are in product code HQC (Unit, Phacofragmentation). 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 Carl Zeiss Meditec Cataract Technologies’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

FIG. 1 — Carl Zeiss Meditec Cataract Technologies by year, 2026–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Carl Zeiss Meditec Cataract Technologies’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Carl”

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

Carl Zeiss Meditec, AG 81 Carl Zeiss, Inc. 44 Carl Zeiss Meditec Cataract Technology, Inc. 7 Carl Parker Associates, Inc. 7 Carl Zeiss Surgical GmbH 4 Carl Zeiss Ophthalmic Systems, Inc. 2 Carl Zeiss Suzhou Co., Ltd. 2 Carl Zeiss Jena GmbH 1 Carl Zeiss Vision GmbH 1 Carl Schuh 1 Carl Zeiss Meditec Production, LLC 1

Carl Zeiss Meditec Cataract Technologies

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Carl”