Benvenue Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Benvenue Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Trivergent Spinal Fixation System, Luna XD Ti Interbody Fusion System, Luna 3D GEN2 Interbody Fusion System
8
Total
8
Cleared
0
Denied
Benvenue Medical, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Historical record: 8 cleared submissions from 2007 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Benvenue Medical, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Mcra, LLC and Musculoskeletal Clinical Regulatory Advisers, LLC.
FDA 510(k) Regulatory Record - Benvenue Medical, Inc.
8 devices
Cleared
Oct 21, 2020
Trivergent Spinal Fixation System
Orthopedic
145d
Cleared
Jul 02, 2020
Luna XD Ti Interbody Fusion System
Orthopedic
230d
Cleared
May 23, 2019
Luna 3D GEN2 Interbody Fusion System
Orthopedic
154d
Cleared
Nov 17, 2016
Luna 3D Interbody Fusion System
Orthopedic
78d
Cleared
Nov 20, 2014
LUNA INTERBODY SYSTEM
Orthopedic
118d
Cleared
Aug 14, 2014
KIVA VCF TREATMENT SYSTEM
Orthopedic
104d
Cleared
Jan 24, 2014
KIVA VCF TREATMENT SYSTEM
Orthopedic
137d
Cleared
Jul 10, 2007
BENVENUE VCF OSTEO COIL SYSTEM
Orthopedic
160d