Wound Geni NPWT System

FDA 510(k) K254019 · Bechtel Medical, Inc.

Substantially Equivalent

510(k) numberK254019

Submission

Device name
Wound Geni NPWT System
Applicant
Bechtel Medical, Inc.
Collegeville, PA, US
Received
December 15, 2025
Decision date
May 4, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OMP – Negative Pressure Wound Therapy Powered Suction Pump
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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.

Other 510(k)s with product code OMP

510(k)DeviceApplicantDecision
K261338RENASYS DYNAFLOW Kit (66807741)OMP · Traditional Smith & Nephew Medical, Ltd.09/11/2026SE
K253263ConvaVAC™ Negative Pressure Wound Therapy SystemOMP · Traditional Convatec Limited, Gdc Building06/24/2026SE
K253199Curasys 2 (EMDN0003)OMP · Traditional CG Bio Co., Ltd.06/23/2026SE
K260646Renasys Edge (66803126)OMP · Traditional Smith & Nephew Medical, Ltd.05/27/2026SE
K261291Nisus NPWT Canister 500-mL (CPC-500)OMP · Special Cork Medical05/21/2026SE
K253429Genadyne ASTRA NPWTOMP · Traditional Genadyne Biotechnologies, Inc.03/12/2026SE
K250586Prospera Spectruum Negative Pressure Wound Therapy Black Foam Kits and White Foam…OMP · Traditional Deroyal Industries, Inc.11/21/2025SE
K251646extriCARE® 1000 Negative Pressure Wound Therapy SystemOMP · Traditional Alleva Medical Devices10/03/2025SE
K251826RENASYS WOUND+ Dressing Kit with AIRLOCK TechnologyOMP · Traditional Smith & Nephew Medical, Ltd.09/11/2025SE
K243187Nisus ONE Negative Pressure Wound Therapy System (OCMPP-100)OMP · Traditional Cork Medical06/27/2025SE

Questions and answers

When was Wound Geni NPWT System cleared by the FDA?

Wound Geni NPWT System (K254019) received a 510(k) decision of Substantially Equivalent on May 4, 2026, 140 days after the submission was received.

What is the product code of K254019?

The FDA product code is OMP – Negative Pressure Wound Therapy Powered Suction Pump, a Class II (moderate risk) device regulated under 21 CFR 878.4780.