Medsource International, LLC is one of 16075 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medsource International, LLC - FDA 510(k) Cleared Devices
Recent clearances: The MedSource TrueSafe Blood Control I.V. Safety Catheter, and the MedSource ClearSafe Blood Control I.V. Safety Catheter, MedSource TrueSafe Safety IV Catheter, MedSource TrueSafe Comfort Safety IV Catheter, MedSource Sharps Dart
9
Total
9
Cleared
0
Denied
Medsource International, LLC has 9 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Last cleared in 2023. Active since 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medsource International, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory Technology Services, LLC and Eqact, Inc..
FDA 510(k) Regulatory Record - Medsource International, LLC
9 devices
Cleared
Sep 15, 2023
The MedSource TrueSafe Blood Control I.V. Safety Catheter, and the MedSource...
General Hospital
270d
Cleared
Nov 03, 2016
MedSource TrueSafe Safety IV Catheter, MedSource TrueSafe Comfort Safety IV...
General Hospital
127d
Cleared
May 08, 2015
MedSource Sharps Dart
General Hospital
87d
Cleared
Apr 22, 2014
MEDSOURCE SELECTABLE IV SET
General Hospital
60d
Cleared
Apr 03, 2014
MEDSOURCE IV ADMINISTRATION SET 72 MEDSOURCE IV ADMINISTRATION SET,...
General Hospital
44d
Cleared
Jan 31, 2014
MEDSOURCE IV SAFETY CATHETER
General Hospital
247d
Cleared
Jul 11, 2012
MEDSOURCE IV ADMINSTRATION SET
General Hospital
149d
Cleared
Oct 27, 2008
MEDSOURCE ENDOTRACHEAL TUBE (WITH AND WITHOUT CUFF)
Anesthesiology
262d
Cleared
Aug 26, 2008
MEDSOURCE CPR MASK WITH & WITHOUT OXYGEN PORT
Anesthesiology
88d