FDA applicant

Medtech Intl., Inc.

Mchenry, IL6 decisions1978–19920 recalls

FDA records 6 decisions for Medtech Intl., Inc. (Mchenry, IL) from 1978 to 1992: 6 510(k) clearances. Most are in product codes KGO (Surgeon'S Gloves) and FLN (Monitor, Electric For Gravity Flow Infusion…). 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 and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Medtech Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Medtech”

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

Medtech Products, Inc. 14 Medtech S.A 8 Medtech S.A.S 4 Medtech Industries, Inc. 4 The Medtech Group, Inc. 2 Medtech Instruments 2 Medtech Systems, Inc. 1

Medtech Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Medtech”