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.
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
Cleared
Aug 25, 1997
SLEEP-IN BONE SCREW SYSTEM
Dental
84d
Cleared
Apr 23, 1997
IN-FAST BONE SCREW SYSTEM/IN-FAST BONE SCREW INSERTER/IN-FAST BONE SCREW
Orthopedic
89d
Cleared
Feb 13, 1997
IN-TAC BONE ANCHOR SYSTEM
Orthopedic
70d
Cleared
Aug 19, 1996
UROTAC BONE ANCHOR INSERTER
Orthopedic
61d