Customed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Customed, Inc. - FDA 510(k) Cleared Devices
36
Total
26
Cleared
0
Denied
Customed, Inc. has 26 FDA 510(k) cleared medical devices. Based in Carolina Puerto Rico, US.
Historical record: 26 cleared submissions from 1990 to 1998.
Browse the FDA 510(k) cleared devices submitted by Customed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Customed, Inc.
36 devices
Cleared
Jan 05, 1998
FANFOLD DRAPE 41 X 57 PRODUCT NO. 900-633, RECORDER NO. 0633
General Hospital
24d
Cleared
Dec 04, 1997
GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)
General Hospital
195d
Cleared
Nov 25, 1996
SUCTION CATHETER TRAY PRODUCT NO. 900277
General & Plastic Surgery
49d
Cleared
Oct 04, 1996
URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)
Gastroenterology & Urology
88d
Cleared
Sep 27, 1996
CUSTOMED BLOOD EXTRACTION KIT
Chemistry
87d
Cleared
May 09, 1996
UNIVERSAL DRAINAGE TRAY
Gastroenterology & Urology
24d
Cleared
Oct 02, 1995
STERIMED STERIZATION WRAPPER (NON-STERILE)
General Hospital
56d
Cleared
Apr 18, 1995
WOUND CLOSURE/LACERATION TRAY
General & Plastic Surgery
84d
Cleared
Sep 08, 1994
FOLEY CATHETERIZATION TRAY
Gastroenterology & Urology
127d
Cleared
Aug 27, 1993
IV PREP KIT (NON-STERILE)
General & Plastic Surgery
337d
Cleared
Aug 27, 1993
IV PREP KIT W/O DRESSING (NON-STERILE)
General & Plastic Surgery
337d
Cleared
Jul 14, 1993
BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560
Anesthesiology
139d