510(k) Report

FDA applicant

Tower Mfg. Co., Inc.

San Antonio, TX1 decision1987–19870 recalls

FDA records 1 decision for Tower Mfg. Co., Inc. (San Antonio, TX) in 1987: 1 510(k) clearance. All are in product code GEH (Unit, Cryosurgical, Accessories). 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 Tower Mfg. Co., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tower Mfg. Co., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tower Mfg. Co., 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?

  • GEHUnit, Cryosurgical, Accessories1decision

What has FDA decided for it lately?

  • K872796Additions to WSL Nitrospray Cryosurgical UnitsTower Mfg. Co., Inc. · 1987

The one decision as Tower Mfg. Co., Inc. →

Other applicant names beginning “Tower”

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

Tower Products, Inc. 3Tower Rubber Industries Sdn. Bhd. 2Tower Laboratories, Ltd. 1Tower Marketing Sdn. Bhd. 1Tower Stopper, Inc. 1