FDA applicant

Dolphin Imaging Systems

Valencia, CA1 decision1991–19910 recalls

FDA records 1 decision for Dolphin Imaging Systems (Valencia, CA) in 1991: 1 510(k) clearance. All are in product code EAG (Cephalometer). 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, dental panel, where it files most

How often FDA has decided Dolphin Imaging Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dolphin Imaging Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Dolphin”

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

Dolphin Medical, Inc. 12 Dolphin Medical Technologies, Inc. 2 Dolphin Medical Imaging, LLC 1

Dolphin Imaging Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Dolphin”