510(k) Report

FDA applicant

Nautilus Sports/Medical Industries, Inc.

Deland, FL1 decision1986–19860 recalls

FDA records 1 decision for Nautilus Sports/Medical Industries, Inc. (Deland, FL) in 1986: 1 510(k) clearance. All are in product code IKK (System, Isokinetic Testing And Evaluation). 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, physical medicine panel, where it files most

How often FDA has decided Nautilus Sports/Medical Industries, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nautilus Sports/Medical Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Nautilus”

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