Exelint International, Co.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251089EXEL Disposable Syringe; EXEL Disposable Syringe with Needle; EXEL Disposable Syringe with Secure ToDecember 12, 2025
K152183EXELINT SecureTouch Safety Hypodermic NeedleNovember 2, 2015
K101309EXELINT ALUMINUM HUB BLUNT NEEDLESOctober 20, 2010
K020189EXEL BUTTERFLY SCALP VEIN SETMarch 27, 2003
K010197EXEL SECURE TOUCH SAFETY (P.S.V.) SCALP VEIN SETMay 14, 2001
K003627EXEL SECURE TOUCH SAFETY A.V. FISTULA NEEDLE SETFebruary 8, 2001
K001496A.V. FISTULA NEEDLEAugust 1, 2000