Teleflex, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Teleflex, Inc. - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Teleflex, Inc. has 10 FDA 510(k) cleared anesthesiology devices. Based in Jeffrey, US.
Historical record: 10 cleared submissions from 1986 to 2016.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Teleflex, Inc.
10 devices
Cleared
Jun 21, 2016
ARROW FlexBlock Continuous Peripheral Nerve Block Catheter Kit/Set
Anesthesiology
183d
Cleared
Mar 27, 2015
FLEXTIP PLUS EPIDURAL CATHETER
Anesthesiology
436d
Cleared
Nov 24, 2014
CONCHASMART COLUMN
Anesthesiology
130d
Cleared
Sep 24, 2014
CONCHASMART BREATHING CIRCUIT
Anesthesiology
203d
Cleared
Mar 06, 2014
CONCHATHERM NEPTUNE HEATED HUMIDIFIER, COMFORT FLO HUMIDIFICATION SYSTEM,...
Anesthesiology
253d
Cleared
Feb 21, 2013
PERCUTANEOUS INTRODUCER KIT
Cardiovascular
57d
Cleared
Jun 20, 2012
CONTINUOUS PERIPHERAL NERVE BLOCK CATHETER KIT AND SET
Anesthesiology
41d
Cleared
May 16, 2012
FLEXTIP PLUS CLOSED TIP EPIDURAL CATHERTER
Anesthesiology
518d
Cleared
Jun 19, 1986
MODIFIED TELEFLEX MEDICAL INTRODUCER CATHETER
Cardiovascular
30d
Cleared
May 20, 1986
PEEL AWAY & SPLIT SHEATH PERCU CATH INTRODUCER SET
Cardiovascular
112d