510(k) Report

FDA applicant

Taylor Bio-Medical, Inc.

Alpena, MI1 decision1993–19930 recalls

FDA records 1 decision for Taylor Bio-Medical, Inc. (Alpena, MI) in 1993: 1 510(k) clearance. All are in product code FRA (Purifier, Air, Ultraviolet, Medical). 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, general hospital panel, where it files most

How often FDA has decided Taylor Bio-Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Taylor Bio-Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Taylor Bio-Medical, 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 “Taylor”

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