FDA applicant

Atlantis Scientific Corp.

Indianapolis, IN1 decision1984–19840 recalls

FDA records 1 decision for Atlantis Scientific Corp. (Indianapolis, IN) in 1984: 1 510(k) clearance. All are in product code IKE (Transducer, Miniature Pressure). 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 Atlantis Scientific Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Atlantis Scientific Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Atlantis”

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

Atlantis Components, Inc. 18 Atlantis Diagnostics Intl., Inc. 3 Atlantis Luminescent Products, LLC 1

Atlantis Scientific Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Atlantis”