Medical Device Manufacturer · US , Minneapolis , MN

Coloplast Manufacturing Us, LLC

4 submissions · 4 cleared · Since 2007
4
Total
4
Cleared
0
Denied

Coloplast Manufacturing Us, LLC has 4 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Historical record: 4 cleared submissions from 2007 to 2010. Primary specialty: Gastroenterology & Urology.

Browse the FDA 510(k) cleared devices submitted by Coloplast Manufacturing Us, LLC Filter by specialty or product code using the sidebar.

4 devices
1–4 of 4
SELF CATH CATHETER
K100878 · EZD Catheter, Straight · Gastroenterology & Urology
May 2010 57d
DIGITEX SUTURE DELIVERY SYSTEM, MODEL 52025, DIGITEX SUTURE CARTRIDGE (SIZE O), MODEL 52026, DIGITEX SUTURE CARTRIDGE
K093112 · GAW Suture, Nonabsorbable, Synthetic, Polypropylene · General & Plastic Surgery
Feb 2010 123d
VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM
K082640 · OTM Mesh, Surgical, For Stress Urinary Incontinence, Male · Gastroenterology & Urology
Oct 2008 37d
SELF-CATH CS CLOSED URINARY CATHETERIZATION SYSTEM
K070939 · FCM Tray, Catheterization, Sterile Urethral, With Or Without Catheter (kit) · Gastroenterology & Urology
Jun 2007 58d
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All4 Gastroenterology & Urology 3 General & Plastic Surgery 1