FDA applicant

Lloyd V. Ziemendorf

Niagara Falls, NY1 decision1997–19970 recalls

FDA records 1 decision for Lloyd V. Ziemendorf (Niagara Falls, NY) in 1997: 1 510(k) clearance. All are in product code EHS (Cushion, Denture, Over The Counter). 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, dental panel, where it files most

How often FDA has decided Lloyd V. Ziemendorf’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lloyd V. Ziemendorf since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Lloyd”

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

Lloyd Linden, Inc. 1 Lloyd Baum Center, Inc. 1

Lloyd V. Ziemendorf

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Lloyd”