Link America, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Link America, Inc. - FDA 510(k) Cleared Devices
21
Total
19
Cleared
0
Denied
Link America, Inc. has 19 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 19 cleared submissions from 1984 to 1997.
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 - Link America, Inc.
21 devices
Cleared
Oct 22, 1997
LINK, ACETABULAR REVISION MESH CUP
Orthopedic
90d
Cleared
Dec 09, 1996
ELLIS EXTERNAL MINI-FIXATOR SYSTEM
Orthopedic
32d
Cleared
Feb 14, 1996
LINK MP RECONSTRUCTION HIP
Orthopedic
90d
Cleared
Jan 26, 1996
SLED UNICOMPARTMENT KNEE SYSTEM
Orthopedic
142d
Cleared
Apr 19, 1994
LINK CERAMIC HEADS 12/14 X 32MM
Orthopedic
385d
Cleared
Mar 28, 1994
LINK CERAMIC HEADS 14/16 X 32MM
Orthopedic
363d
Cleared
May 18, 1992
FELDMUHLE CERAMIC HEAD
Orthopedic
89d
Cleared
Apr 29, 1992
RADIUS OSTEOTOMY PLATES
Orthopedic
188d
Cleared
Apr 28, 1992
SCHWABE RADIUS PLATES
Orthopedic
187d
Cleared
Mar 13, 1990
LINK GIEBEL BLADE PLATE SYSTEM
Orthopedic
183d
Cleared
Sep 16, 1987
LINK (R) AMERICAN-TYPE BONE STAPLE SYSTEM
Orthopedic
16d
Cleared
May 14, 1987
SMILJANIC BONE REPOSITIONING FORCEPS
General & Plastic Surgery
24d