510(k) Report

FDA applicant

Tower Products, Inc.

Mchenry, IL3 decisions1977–19770 recalls

FDA records 3 decisions for Tower Products, Inc. (Mchenry, IL) in 1977: 3 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and KCT (Sterilization Wrap Containers, Trays…). 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 Tower Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tower Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tower Products, 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?

  • FRGWrap, Sterilization1decision
  • KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories1decision
  • JOJIndicator, Physical/Chemical Sterilization Process1decision

What has FDA decided for it lately?

  • K771146Steoility Testing VesselTower Products, Inc. · 1977
  • K771348Econowrap Paper C.S.R. WrapTower Products, Inc. · 1977
  • K770912TiprotectorTower Products, Inc. · 1977

All 3 as Tower Products, Inc. →

Other applicant names beginning “Tower”

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

Tower Rubber Industries Sdn. Bhd. 2Tower Laboratories, Ltd. 1Tower Marketing Sdn. Bhd. 1Tower Stopper, Inc. 1Tower Mfg. Co., Inc. 1