Shippert Medical Technologies Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Shippert Medical Technologies Corp. - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
Shippert Medical Technologies Corp. has 13 FDA 510(k) cleared medical devices. Based in Englewood, US.
Historical record: 13 cleared submissions from 1995 to 2010.
Browse the FDA 510(k) cleared devices submitted by Shippert Medical Technologies Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Shippert Medical Technologies Corp.
13 devices
Cleared
Aug 06, 2010
TISSU TRANS FILTRON SYRINGE FILL
General & Plastic Surgery
9d
Cleared
Dec 04, 2009
TISSU TRANS FILTRON, MODELS 3-TT-FILTRON 2000-500
General & Plastic Surgery
113d
Cleared
Aug 17, 2009
TISSU TRANS HARVEST TUBING
General Hospital
42d
Cleared
Jul 13, 2005
TISSU-TRANS
General Hospital
106d
Cleared
Mar 04, 1997
EXPANDACELL EYE SPEAR, EYE WICK, WICK DRAIN AND CORNEAL SHIELD
Ophthalmic
90d
Cleared
Dec 09, 1996
EXPANDACELL ANTI-FOG INSTRUMENT WIPE (WITH ALCOHOL)/(WITHOUT)
General & Plastic Surgery
39d
Cleared
Nov 26, 1996
MUSCLE WAND, A DEVICE FOR DEEP PRESSURE MUSCLE MASSAGE
Physical Medicine
71d
Cleared
Aug 01, 1996
EXPANDACELL INJECTO-PAK
Ear, Nose, Throat
59d
Cleared
Apr 01, 1996
EXPANDACELL INSTRUMENT WIPE
General & Plastic Surgery
48d
Cleared
Feb 27, 1996
EXPANDACELL INJECTO-PAK NASAL PACK
Ear, Nose, Throat
41d
Cleared
Dec 22, 1995
EXPANDACELL ANATOMICAL POSTERIOR NASAL PACK W/& WITHOUT AIRWAY
Ear, Nose, Throat
15d
Cleared
Nov 27, 1995
EXPANDACELL INJECTO-PAK NASAL PACK
Ear, Nose, Throat
35d