510(k) Report

FDA applicant

The Medtech Group, Inc.

South Planifield, NJ2 decisions1986–19890 recalls

FDA records 2 decisions for The Medtech Group, Inc. (South Planifield, NJ) from 1986 to 1989: 2 510(k) clearances. Most are in product codes FMF (Syringe, Piston) and CAE (Airway, Oropharyngeal, Anesthesiology). 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 Medtech Group, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for The Medtech Group, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • FMFSyringe, Piston1decision
  • CAEAirway, Oropharyngeal, Anesthesiology1decision

What has FDA decided for it lately?

  • K895203EN-Trap SyringeThe Medtech Group, Inc. · 1989
  • K862199Medtech C.P.R. MaskThe Medtech Group, Inc. · 1986

All 2 as The Medtech Group, Inc. →

Other applicant names beginning “The”

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

Medtech Products, Inc. 14Medtech S.A 8Medtech Intl., Inc. 6Medtech S.A.S 4Medtech Industries, Inc. 4Medtech Instruments 2Medtech Systems, Inc. 1