FDA applicant

Harbor Medical Devices, Inc.

Boston, MA7 decisions1988–19890 recalls

FDA records 7 decisions for Harbor Medical Devices, Inc. (Boston, MA) from 1988 to 1989: 7 510(k) clearances. Most are in product codes LJT (Port & Catheter, Implanted, Subcutaneous…) and DQR (Cannula, Catheter). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Harbor Medical Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Harbor”

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

Harbor Medtech, Inc. 2 Harbor Medical, Inc. 2

Harbor Medical Devices, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Harbor”