FDA applicant

Meadox Surgimed, Inc.

Oakland, NJ24 decisions1984–19950 recalls

FDA records 24 decisions for Meadox Surgimed, Inc. (Oakland, NJ) from 1984 to 1995: 24 510(k) clearances. Most are in product codes KNW (Instrument, Biopsy) and DQX (Wire, Guide, 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, gastroenterology and urology panel, where it files most

How often FDA has decided Meadox Surgimed, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Meadox Surgimed, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Meadox Surgimed, 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 “Meadox”

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

Meadox Medicals, Div. Boston Scientific Corp. 54

Meadox Surgimed, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Meadox”