Hand Innovations, Inc. is one of 24550 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hand Innovations, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM, SHOULDER FIXATION SYSTEM, MODIFICATION TO SMALL BONE FIXATION SYSTEM
10
Total
10
Cleared
0
Denied
Hand Innovations, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in Miami, US.
Historical record: 10 cleared submissions from 2000 to 2005.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hand Innovations, Inc.
10 devices
Cleared
Apr 26, 2005
DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM
Orthopedic
12d
Cleared
Sep 30, 2004
SHOULDER FIXATION SYSTEM
Orthopedic
62d
Cleared
Jul 30, 2004
MODIFICATION TO SMALL BONE FIXATION SYSTEM
Orthopedic
88d
Cleared
Jul 01, 2004
FRAGMENT PLATE SYSTEM, SCREWS, PINS AND K-WIRES
Orthopedic
66d
Cleared
Jan 15, 2004
SMALL BONE FIXATION SYSTEM
Orthopedic
83d
Cleared
Oct 01, 2003
DISTAL RADIUS FRACTURE REPAIR SYSTEM
Orthopedic
29d
Cleared
Apr 01, 2003
HAND INNOVATIONS, INC. DISTAL RADIUS FRACTURE REPAIR SYSTEM
Orthopedic
70d
Cleared
Dec 05, 2002
DISTAL RADIUS FRACTURE REPAIR SYSTEM
Orthopedic
87d
Cleared
Dec 20, 2001
INTRAMEDULLARY FIXATION SYSTEM FOR THE HAND
Orthopedic
66d
Cleared
Dec 05, 2000
DISTAL VOLAR RADIUS FRACTURE REPAIR SYSTEM
Orthopedic
90d