510(k) Report

FDA applicant

Implantable Devices

Tampa, FL1 decision2002–20020 recalls

FDA records 1 decision for Implantable Devices (Tampa, FL) in 2002: 1 510(k) clearance. All are in product code DXC (Clamp, Vascular). 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, cardiovascular panel, where it files most

How often FDA has decided Implantable Devices’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Implantable Devices since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Implantable Devices’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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