Cleared Traditional

Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory

K250586 · Deroyal Industries, Inc. · General & Plastic Surgery
Nov 2025
Decision
267d
Days
Class 2
Risk

About This 510(k) Submission

K250586 is an FDA 510(k) clearance for the Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam Accessory, a Negative Pressure Wound Therapy Powered Suction Pump (Class II — Special Controls, product code OMP), submitted by Deroyal Industries, Inc. (Powell, US). The FDA issued a Cleared decision on November 21, 2025, 267 days after receiving the submission on February 27, 2025. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4780.

Submission Details

510(k) Number K250586 FDA.gov
FDA Decision Cleared SESE
Date Received February 27, 2025
Decision Date November 21, 2025
Days to Decision 267 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code OMP — Negative Pressure Wound Therapy Powered Suction Pump
Device Class Class II — Special Controls
CFR Regulation 21 CFR 878.4780
Definition For Wound Management Via Application Of Continual Or Intermittent Negative Pressure To The Wound For Removal Of Fluids, Including Wound Exudate, Irrigation Fluids, And Infectious Materials. The Device Is Indicated For Management Of Chronic, Acute, Traumatic, Subacute And Dehisced Wounds, Partial-thickness Burns, Ulcers (such As Diabetic Or Pressure), Flaps And Grafts.

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