Buckman Co., Inc. - FDA 510(k) Cleared Devices
111
Total
104
Cleared
0
Denied
Buckman Co., Inc. has 104 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 104 cleared submissions from 1983 to 1998. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Buckman Co., Inc. Filter by specialty or product code using the sidebar.
111 devices
Cleared
Jun 25, 1998
CROSS MEDICAL BONE PLATE SYSTEM/ CM BONE PLATE SYSTEM/CROSS TI BONE PLATE SYSTEM
Orthopedic
811d
Cleared
Jun 08, 1998
FUTURELASE 3000/3002 ERBIUM LASER SYSTEM
General & Plastic Surgery
175d
Cleared
May 27, 1997
ORTHOCHUCK
General & Plastic Surgery
215d
Cleared
Jan 16, 1997
SYNERGY(TM) TI POSTERIOR SPINAL SYSTEM
Orthopedic
737d
Cleared
Apr 18, 1996
WEBB-MORLEY SPINE SYSTEM
Orthopedic
79d
Cleared
Jan 25, 1996
KSF POSTERIOR SPINGAL FIXATOR FOR SEVERE SPONDYLOLISTHESIS
Orthopedic
328d
Cleared
Dec 19, 1995
IMAGN(TM) 2000 SYSTEM
Hematology
391d
Cleared
Oct 19, 1995
VOLUMET CD4 + AND CD8 + T LYMPHOCYTE COUNT TEST KIT
Hematology
654d
Cleared
Oct 18, 1995
LIHTAN 532 LASER
General & Plastic Surgery
222d
Cleared
Feb 09, 1995
VANGUARD SERIES GAS REGULATORS
Anesthesiology
244d
Cleared
Oct 20, 1994
ANTERIOR SPINE SYSTEM
Orthopedic
402d
Cleared
Apr 12, 1994
LAPAROSCOPY INSTRUMENTS
General & Plastic Surgery
368d
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