Biopro, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biopro, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Shotel Ankle Arthrodesis Nail System, BioPro Foot Plating Systems, BIOPRO - INFINITY PLATE ANCHOR SYSTEM
41
Total
35
Cleared
0
Denied
Biopro, Inc. has 35 FDA 510(k) cleared orthopedic devices. Based in Port Huron, US.
Historical record: 35 cleared submissions from 1987 to 2017.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Engineering Consulting Services, Inc. and Convergent Clinical,Inc..
FDA 510(k) Regulatory Record - Biopro, Inc.
41 devices
Cleared
Sep 14, 2017
Shotel Ankle Arthrodesis Nail System
Orthopedic
266d
Cleared
Jun 16, 2017
BioPro Foot Plating Systems
Orthopedic
263d
Cleared
Oct 24, 2013
BIOPRO - INFINITY PLATE ANCHOR SYSTEM
Orthopedic
73d
Cleared
Jun 18, 2013
BIOPRO KWICK-WIRE UNIVERSAL SCREW SYSTEM
Orthopedic
131d
Cleared
Oct 30, 2012
BIOPRO HEMI-EDGE TOE SYSTEM
Orthopedic
117d
Cleared
Dec 03, 2010
BIOPRO POLAR HEAD
Orthopedic
261d
Cleared
Jun 03, 2010
MODIFICATION TO HBS HEADLESS BONE SCREW
Orthopedic
51d
Cleared
May 22, 2009
BIOPRO FEMORAL HEADS
Orthopedic
114d
Cleared
Mar 18, 2009
BIOPRO K-WIRE, MODELS 16863, 17231, 17232, 18577, 18682-18685
Orthopedic
113d
Cleared
Dec 15, 2008
BIOPRO BIPOLAR HEAD, MODELS 18130-18152
Orthopedic
90d
Cleared
Aug 05, 2008
BIOPRO GO-EZ SCREW
Orthopedic
105d
Cleared
Oct 29, 2007
BIOPRO MEMORY STAPLE, MODELS 18062-18073
Orthopedic
73d
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