FDA applicant

The Boston Medical Group

Walker, MI5 decisions1982–19820 recalls

FDA records 5 decisions for The Boston Medical Group (Walker, MI) in 1982: 5 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and BRZ (Set, Blood Transfusion). 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 The Boston Medical Group’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Boston Medical Group since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like The Boston Medical Group’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “The”

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

Boston Scientific Corp 809 Boston Scientific Scimed, Inc. 40 Boston Medical Products, Inc. 33 Boston Scientific, Target 19 Boston Surgical Products, Inc. 17 Boston Biomedica, Inc. 12 Boston Scientific Neuromodulation 11 Boston Pacific Medical, Inc. 11 Boston Medical Corp. 8 Boston Aesthetics, Inc. 6 Boston Scientific/Medi-Tech 5 Boston Scientific /International Technologies 5

The Boston Medical Group

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “The”