Renovis Surgical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Renovis Surgical Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: S128 Anterior Lumbar Interbody Fusion (ALIF) System
7
Total
7
Cleared
0
Denied
Renovis Surgical Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Ashland, US.
Historical record: 7 cleared submissions from 2014 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Renovis Surgical Technologies, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MEDIcept, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Renovis Surgical Technologies, Inc.
7 devices
Cleared
Jun 14, 2018
S128 Anterior Lumbar Interbody Fusion (ALIF) System
Orthopedic
108d
Cleared
Sep 25, 2015
Renovis Anterior Cervical Plate System
Orthopedic
51d
Cleared
May 11, 2015
Renovis Surgical Hip Replacement System
Orthopedic
140d
Cleared
Nov 04, 2014
RENOVIS SURGICAL POROUS ACETABULAR CUP SYSTEM
Orthopedic
134d
Cleared
Oct 15, 2014
RENOVIS S134 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
Orthopedic
75d
Cleared
Sep 02, 2014
RENOVIS CEMENTED HIP SYSTEM
Orthopedic
98d
Cleared
Mar 27, 2014
S128 ANTERIOR LUMBAR INTERBODY FUSION (ALIF) SYSTEM
Orthopedic
71d