FDA applicant

Dolphin Medical Technologies, Inc.

Sarasota, FL2 decisions1998–19990 recalls

FDA records 2 decisions for Dolphin Medical Technologies, Inc. (Sarasota, FL) from 1998 to 1999: 2 510(k) clearances. All are in product code HWC (Screw, Fixation, Bone). Its devices cite 14 predicates, 0 of them its own earlier devices. 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, orthopedic panel, where it files most

How often FDA has decided Dolphin Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dolphin Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dolphin Medical Technologies, 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 “Dolphin”

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

Dolphin Medical, Inc. 12 Dolphin Medical Imaging, LLC 1 Dolphin Imaging Systems 1

Dolphin Medical Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Dolphin”