Sgarlato Laboratories, Inc. is one of 9846 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sgarlato Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PAIN CONTROL INFUSION PUMP, THREADED FIXATION PIN
8
Total
8
Cleared
0
Denied
Sgarlato Laboratories, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Jose, US.
Historical record: 8 cleared submissions from 1989 to 2005. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Sgarlato Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sgarlato Laboratories, Inc.
8 devices
Cleared
Mar 30, 2005
SGARLATO LABS PAINFREE PUMP AND PAIN CONTROL INFUSION PUMP
General Hospital
132d
Cleared
Mar 19, 1999
PAIN CONTROL INFUSION PUMP
General Hospital
66d
Cleared
Oct 21, 1998
THREADED FIXATION PIN
Orthopedic
62d
Cleared
Jan 26, 1994
FIRST MPJ CONTINUOUS PASSIVE MOTION DEVICE
Physical Medicine
404d
Cleared
Aug 02, 1993
O'BRIEN GONIOMETER
Neurology
234d
Cleared
Oct 23, 1992
LUNDEEN SUBTALAR PEG IMPLANT
Orthopedic
161d
Cleared
May 29, 1991
SGARLATO FLEXIBLE HINGE TOE IMPLANT
Orthopedic
153d
Cleared
May 18, 1989
SGARLATO LESSER TOE IMPLANT
Orthopedic
185d