FDA applicant

Cure Point Therapeutics, Inc.

Cheyenne, WY1 decision2024–20240 recalls

FDA records 1 decision for Cure Point Therapeutics, Inc. (Cheyenne, WY) in 2024: 1 510(k) clearance. All are in product code ILY (Lamp, Infrared, Therapeutic Heating). 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, physical medicine panel, where it files most

How often FDA has decided Cure Point Therapeutics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Cure Point Therapeutics, Inc. by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Cure”

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

Cure Medical, LLC 4

Cure Point Therapeutics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cure”