510(k) Report

FDA applicant

Vital Concepts, Inc.

Grand Rapids, MI4 decisions1994–200310 recalls

FDA records 4 decisions for Vital Concepts, Inc. (Grand Rapids, MI) from 1994 to 2003: 4 510(k) clearances. Most are in product codes BYY (Tube, Aspirating, Flexible, Connecting) and HRX (Arthroscope). 10 recalls are 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 Vital Concepts, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vital Concepts, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vital Concepts, 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 “Vital”

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