Influence, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Influence, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Influence, Inc. has 16 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Historical record: 16 cleared submissions from 1996 to 1999. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Influence, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Influence, Inc.
16 devices
Cleared
Aug 27, 1999
REPOSE BONE SCREW SYSTEM
Dental
472d
Cleared
Aug 12, 1999
CRYO-MONO CRYOGENIC SYSTEM, MODEL CRYO-MONO WITH TUF PROBE
General & Plastic Surgery
78d
Cleared
Jul 30, 1999
STAPLETAC BONE ANCHOR SYSTEM
Orthopedic
23d
Cleared
Jul 01, 1999
CRYO-MONO CRYOGRNIC SYSTEM
General & Plastic Surgery
90d
Cleared
Feb 16, 1999
MICROTAC-BONE ANCHOR SYSTEM
Orthopedic
28d
Cleared
Feb 01, 1999
STRAIGHT-IN-ORTHOPEDIC BONE SCREW FIXATION SYSTEM
Orthopedic
20d
Cleared
Nov 24, 1998
IN-PROBE II URODYNAMIC SYSTEM
Gastroenterology & Urology
63d
Cleared
Aug 31, 1998
SHORT STRAIGHT-IN BONE SCREW FIXATION SYSTEM
Orthopedic
74d
Cleared
Jul 28, 1998
INFLUENCE CLIP SYSTEM
General & Plastic Surgery
82d
Cleared
Mar 27, 1998
TRIANGLE SLING
Gastroenterology & Urology
46d
Cleared
Oct 09, 1997
STRAIGHT-IN BONE SCREW FIXATION SYSTEM
Orthopedic
87d
Cleared
Sep 19, 1997
IN-SLING
Gastroenterology & Urology
67d