FDA applicant

Neosci Medical, Inc.

Salt Lake City, UT1 decision2004–20040 recalls

FDA records 1 decision for Neosci Medical, Inc. (Salt Lake City, UT) in 2004: 1 510(k) clearance. All are in product code LJS (Catheter, Intravascular, Therapeutic…). 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 Neosci Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Neosci Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Neosci Medical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?