Exelint International, Co. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Exelint International, Co. has 7 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Latest FDA clearance: Dec 2025. Active since 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Exelint International, Co. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Exelint International, Co.
7 devices
Cleared
Dec 12, 2025
EXEL Disposable Syringe
General Hospital
246d
Cleared
Nov 02, 2015
EXELINT SecureTouch Safety Hypodermic Needle
General Hospital
89d
Cleared
Oct 20, 2010
EXELINT ALUMINUM HUB BLUNT NEEDLES
General Hospital
163d
Cleared
Mar 27, 2003
EXEL BUTTERFLY SCALP VEIN SET
General Hospital
433d
Cleared
May 14, 2001
EXEL SECURE TOUCH SAFETY (P.S.V.) SCALP VEIN SET
General Hospital
112d
Cleared
Feb 08, 2001
EXEL SECURE TOUCH SAFETY A.V. FISTULA NEEDLE SET
General Hospital
76d
Cleared
Aug 01, 2000
A.V. FISTULA NEEDLE
Gastroenterology & Urology
78d