510(k) Report

FDA applicant

Clear Choice Therapeutics

Raleigh, NC2 decisions2021–20240 recalls

FDA records 2 decisions for Clear Choice Therapeutics (Raleigh, NC) from 2021 to 2024: 2 510(k) clearances. All are in product code OMP (Negative Pressure Wound Therapy Powered…). Its devices cite 2 predicates, 1 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Clear Choice Therapeutics, Inc.”.

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 Clear Choice Therapeutics’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2021: 12024: 1
2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Clear Choice Therapeutics by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Clear Choice Therapeutics’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Clear”

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