Irrimax Corporation - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Irrimax Corporation has 5 FDA 510(k) cleared medical devices. Based in Alpharetta, US.
Latest FDA clearance: Jun 2024. Active since 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Irrimax Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Irrimax Corporation
5 devices
Cleared
Jun 18, 2024
Irrisept Antimicrobial Wound Lavage
General & Plastic Surgery
111d
Cleared
Sep 22, 2022
Irrisept Antimicrobial Wound Lavage
General & Plastic Surgery
6d
Cleared
May 28, 2021
Irrisept Antimicrobial Wound Lavage
General & Plastic Surgery
93d
Cleared
Dec 14, 2020
Irrisept Wound Debridement and Cleansing System
General & Plastic Surgery
130d
Cleared
Feb 04, 2009
IRRISEPT WOUND CLEANSING SYSTEM
General & Plastic Surgery
322d