FDA applicant

Medco Products, Co., Inc.

Tinton Falls, NJ8 decisions1982–19930 recalls

FDA records 8 decisions for Medco Products, Co., Inc. (Tinton Falls, NJ) from 1982 to 1993: 8 510(k) clearances. Most are in product codes GCJ (Laparoscope, General & Plastic Surgery) and IPF (Stimulator, Muscle, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Medco Products, Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medco Products, Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medco Products, Co., 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 “Medco”

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

Medco Instruments, Inc. 1 Medco Mfg. 1

Medco Products, Co., 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 “Medco”