Onyx Medical Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Onyx Medical Corp. - FDA 510(k) Cleared Devices
47
Total
22
Cleared
0
Denied
Onyx Medical Corp. has 22 FDA 510(k) cleared orthopedic devices. Based in Memphis, US.
Historical record: 22 cleared submissions from 1990 to 1994.
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 - Onyx Medical Corp.
47 devices
Cleared
Jul 08, 1994
FACE-IT SHIELD
General Hospital
73d
Cleared
Jun 07, 1994
SPOON PLATE
Orthopedic
428d
Cleared
May 04, 1994
CANNULATED CANCELLOUS SCREW
Orthopedic
394d
Cleared
May 04, 1994
EPIPHYSIS PLATE
Orthopedic
394d
Cleared
May 04, 1994
T-PLATE
Orthopedic
394d
Cleared
May 04, 1994
MINI FRAGMENT PLATE
Orthopedic
219d
Cleared
Apr 25, 1994
BUTTRESS PLATE
Orthopedic
385d
Cleared
Apr 25, 1994
CANNULATED NAVICULAR SCREW
Orthopedic
385d
Cleared
Apr 25, 1994
CLOVERLEAF PLATE
Orthopedic
385d
Cleared
Apr 25, 1994
FOREARM SELF COMPRESSION PLATE
Orthopedic
385d
Cleared
Apr 25, 1994
MULTIPLE FRAGMENT PLATE
Orthopedic
385d
Cleared
Apr 25, 1994
SEMI-TUBULAR PLATE
Orthopedic
385d
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