FDA applicant

Contour Fabricators of Florida, Inc.

St. Petersburg, FL18 decisions1993–19960 recalls

FDA records 18 decisions for Contour Fabricators of Florida, Inc. (St. Petersburg, FL) from 1993 to 1996: 18 510(k) clearances. Most are in product codes FRG (Wrap, Sterilization) and KYZ (Syringe, Irrigating (Non Dental)). 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 Contour Fabricators of Florida, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Contour Fabricators of Florida, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Contour”

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

Contour Medical Technology, Inc. 9 Contour Fabricators, Inc. 8 Contour Electrodes, Inc. 4 Contour Research, LLC 2 Contour, Inc. 1 Contour Healer, LLC 1 Contour Medical Systems, Inc. 1 Contour Technology 1

Contour Fabricators of Florida, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Contour”