Serf is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Serf - FDA 510(k) Cleared Devices
Recent clearances: Novae® Dual Mobility System, Hype® Hip System, BI-MENTUM dual mobility system
4
Total
4
Cleared
0
Denied
Serf has 4 FDA 510(k) cleared medical devices. Based in Round Rock, US.
Last cleared in 2023. Active since 2011. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Serf Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Gloster Biomedical International and BioVera, Inc..
FDA 510(k) Regulatory Record - Serf
4 devices
Cleared
Dec 22, 2023
Novae® Dual Mobility System, Hype® Hip System
Orthopedic
373d
Cleared
Dec 11, 2018
BI-MENTUM dual mobility system
Orthopedic
162d
Cleared
Jan 15, 2015
CI../..X liner for NOVAE Dual Mobility Acetabular Cup
Orthopedic
118d
Cleared
Aug 29, 2011
NOVAE SUNFIT TH DUAL MOBILITY ACETABULAR CUP MODEL SUNFIT TH (METAL-BACK),...
Orthopedic
84d