FDA applicant

Webster Laboratories, Inc.

Walker, MI5 decisions1981–19850 recalls

FDA records 5 decisions for Webster Laboratories, Inc. (Walker, MI) from 1981 to 1985: 5 510(k) clearances. Most are in product codes DRF (Catheter, Electrode Recording, Or Probe…) and LDF (Electrode, Pacemaker, Temporary). 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, cardiovascular panel, where it files most

How often FDA has decided Webster Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Webster Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Webster Laboratories, 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 “Webster”

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

Webster Enterprises, Inc. 1

Webster Laboratories, 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 “Webster”