Acu Med, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acu Med, Inc. - FDA 510(k) Cleared Devices
48
Total
39
Cleared
0
Denied
Acu Med, Inc. has 39 FDA 510(k) cleared orthopedic devices. Based in Beaverton, US.
Historical record: 39 cleared submissions from 1990 to 2002.
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 - Acu Med, Inc.
48 devices
Cleared
Jul 17, 2002
WRIST FUSION PLATE
Orthopedic
83d
Cleared
Dec 19, 2001
POLARUS CAP SCREW
Orthopedic
44d
Cleared
Nov 07, 2001
CONGRUENT BONE PLATE SYSTEM
Orthopedic
86d
Cleared
Feb 04, 2000
ACUMED MODULAR SHOULDER SYSTEM
Orthopedic
191d
Cleared
Jan 13, 2000
ACUMED SUTURE ANCHOR
Orthopedic
77d
Cleared
Mar 16, 1998
ACUMED SUTURE ANCHOR
Orthopedic
63d
Cleared
Mar 17, 1997
ACUMED SUTURE WASHER
Orthopedic
90d
Cleared
Feb 19, 1997
STABLELOC II EXTERNAL FIXATOR
Orthopedic
64d
Cleared
Dec 09, 1996
ACUMED TENSION BAND PIN
Orthopedic
31d
Cleared
Oct 28, 1996
TBD
Orthopedic
84d
Cleared
Oct 10, 1996
EXTREMITY BONE SCREW
Orthopedic
59d
Cleared
Oct 01, 1996
TBD
Orthopedic
54d
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