FDA applicant

Boston Medical Technologies, Inc.

Wakefield, MA3 decisions1999–20010 recalls

FDA records 3 decisions for Boston Medical Technologies, Inc. (Wakefield, MA) from 1999 to 2001: 3 510(k) clearances. All are in product code DPS (Electrocardiograph). Its devices cite 3 predicates, 1 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, cardiovascular panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Boston 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.

See the 510(k) Report

Other applicant names beginning “Boston”

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 The Boston Medical Group 5 Boston Scientific/Medi-Tech 5

Boston Medical Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Boston”