FDA applicant

Taylor Industries, Inc.

New Berlin, WI2 decisions1994–19960 recalls

FDA records 2 decisions for Taylor Industries, Inc. (New Berlin, WI) from 1994 to 1996: 2 510(k) clearances. Most are in product codes DRX (Electrode, Electrocardiograph) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Taylor Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Taylor Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Other applicant names beginning “Taylor”

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

Taylor Instrument Analytics Co. 2 Taylor Medical Equipment 2 Taylor Bio-Medical, Inc. 1 Taylor Corp. 1 Taylor H. Haynes, M.D. 1 Taylor Catheter Holder Mfg. 1 Taylor/Fox Enterprises, LLC 1

Taylor Industries, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Taylor”