Techmedica, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Techmedica, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CKS POROUS COATED FEMORAL COMPONENT, TECHMEDICA CONTINUUM HIP WITH HA COATING, TECHMEDICA CONTINUUM HIP SYSTEM
31
Total
26
Cleared
0
Denied
Techmedica, Inc. has 26 FDA 510(k) cleared orthopedic devices. Based in Mchenry, US.
Historical record: 26 cleared submissions from 1982 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 - Techmedica, Inc.
31 devices
Cleared
Oct 11, 1994
CKS POROUS COATED FEMORAL COMPONENT
Orthopedic
426d
Cleared
Sep 01, 1994
TECHMEDICA CONTINUUM HIP WITH HA COATING
Orthopedic
493d
Cleared
Mar 29, 1994
TECHMEDICA CONTINUUM HIP SYSTEM
Orthopedic
347d
Cleared
Feb 01, 1994
TECHMEDICA STANDARD CEMENTED HIP SYSTEM
Orthopedic
406d
Cleared
Sep 28, 1993
TECHMEDICA STANDARD BIPOLAR SYSTEM
Orthopedic
336d
Cleared
Jul 27, 1993
MULLER STRAIGHT STEM FEMORAL PROSTHESIS
Orthopedic
363d
Cleared
Apr 06, 1993
TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE
Orthopedic
133d
Cleared
Feb 23, 1993
TECHMEDICA CAD/CAM CUSTOM HIP
Orthopedic
718d
Cleared
Feb 05, 1993
TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP
Orthopedic
114d
Cleared
Sep 01, 1992
CONTINUUM KNEE SYSTEM
Orthopedic
237d
Cleared
Jul 17, 1992
TMP MICROPLATING SYSTEM
Orthopedic
112d
Cleared
Jul 15, 1992
MODIFICATION TECHMEDICA MP (MINIPLATING) SYSTEM
Dental
93d