FDA applicant

Cryotherapy Products, Inc.

Terrace Davie, FL1 decision2012–20120 recalls

FDA records 1 decision for Cryotherapy Products, Inc. (Terrace Davie, FL) in 2012: 1 510(k) clearance. All are in product code LKX (Device, Thermal, Hemorrhoids). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

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

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Cryotherapy Products, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Cryotherapy Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?