Medartis, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medartis, Inc. - FDA 510(k) Cleared Devices
Recent clearances: StealthFix Intraosseous Fixation System
5
Total
5
Cleared
0
Denied
Medartis, Inc. has 5 FDA 510(k) cleared medical devices. Based in San Diego, US.
Last cleared in 2023. Active since 2005. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Medartis, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medartis, Inc.
5 devices
Cleared
Aug 30, 2023
StealthFix Intraosseous Fixation System
Orthopedic
27d
Cleared
Oct 21, 2005
MODUS IMF SCREWS 2.0
Dental
84d
Cleared
Aug 23, 2005
APTUS TITANIUM OSTEOSYNTHESIS SYSTEM
Orthopedic
70d
Cleared
Aug 22, 2005
MODUS MODULAR DISTRACTION OSTEOGENESIS SYSTEM
Dental
35d
Cleared
May 05, 2005
MODUS TITANIUM OSTEOSYNTHESIS SYSTEM
Dental
21d