Hollister Incorporated - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Hollister Incorporated has 14 FDA 510(k) cleared gastroenterology & urology devices. Based in Libertyville, US.
Latest FDA clearance: Oct 2025. Active since 2011.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Hollister Incorporated
14 devices
Cleared
Oct 03, 2025
Sleeved IC 3 Family Sleeved IC 3 SWT (name not finalized) Sleeved IC 3 Pocket...
Gastroenterology & Urology
143d
Cleared
May 03, 2024
Sleeved IC 2 Family
Gastroenterology & Urology
184d
Cleared
Dec 08, 2022
Sleeved IC
Gastroenterology & Urology
276d
Cleared
Sep 13, 2022
Female IC (Not Finalized)
Gastroenterology & Urology
307d
Cleared
Jan 27, 2022
Intermittent Catheter (Not Finalized)
Gastroenterology & Urology
262d
Cleared
Dec 13, 2019
VaPro Plus Pocket, VaPro Plus
Gastroenterology & Urology
30d
Cleared
Jul 19, 2019
Infyna Chic
Gastroenterology & Urology
30d
Cleared
Dec 18, 2018
ValPro 2 Plus, VaPro 2 Plus Pocket
Gastroenterology & Urology
27d
Cleared
Jun 22, 2018
VaPro 2 Intermittent Catheter
Gastroenterology & Urology
84d
Cleared
Jan 26, 2017
Onli Intermittent Catheter
Gastroenterology & Urology
73d
Cleared
Sep 09, 2015
VAPRO PLUS POCKET Intermittent Catheter
Gastroenterology & Urology
29d
Cleared
Jan 09, 2015
VaPro Pocket
Gastroenterology & Urology
22d