Corin U.S.A. Limited is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Corin U.S.A. Limited - FDA 510(k) Cleared Devices
Recent clearances: Trinity EVO Acetabular Shell, ApolloHipX (THR.SS.0001), Icona Hip Stem
21
Total
21
Cleared
0
Denied
Corin U.S.A. Limited has 21 FDA 510(k) cleared orthopedic devices. Based in Tampa, US.
Latest FDA clearance: Jun 2025. Active since 2016.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Corin U.S.A. Limited
21 devices
Cleared
Jun 05, 2025
Trinity EVO Acetabular Shell
Orthopedic
267d
Cleared
Jan 07, 2025
ApolloHipX (THR.SS.0001)
Radiology
200d
Cleared
Oct 03, 2024
Icona Hip Stem
Orthopedic
132d
Cleared
Sep 23, 2024
Unity Total Knee System
Orthopedic
115d
Cleared
Jun 26, 2024
Unity Knee PS-C Tibial Insert
Orthopedic
89d
Cleared
Jul 26, 2023
ApolloKnee
Orthopedic
92d
Cleared
Apr 07, 2022
Corin MetaFix™ Hip Stem
Orthopedic
279d
Cleared
Jan 16, 2020
MobiliT Cup
Orthopedic
191d
Cleared
Jul 22, 2019
Revival Modular Hip Stem
Orthopedic
60d
Cleared
Jun 05, 2019
Corin BiPolar-i
Orthopedic
208d
Cleared
Jun 04, 2019
Unity Total Knee System
Orthopedic
167d
Cleared
Jun 15, 2018
Trinity PLUS Acetabular Shell
Orthopedic
296d