Integrity Implants, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Integrity Implants, Inc. - FDA 510(k) Cleared Devices
Recent clearances: LineSider® Spinal System, Toro-L Interbody Fusion System, FlareHawk Interbody Fusion System
11
Total
11
Cleared
0
Denied
Integrity Implants, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Jupiter, US.
Last cleared in 2023. Active since 2019.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Testing Corp, Telos Partners, LLC and Empirical Consulting, LLC.
FDA 510(k) Regulatory Record - Integrity Implants, Inc.
11 devices
Cleared
Aug 07, 2023
LineSider® Spinal System
Orthopedic
111d
Cleared
Mar 25, 2022
Toro-L Interbody Fusion System
Orthopedic
164d
Cleared
Mar 24, 2022
FlareHawk Interbody Fusion System
Orthopedic
35d
Cleared
Dec 23, 2021
Integrity Implants Navigated Instruments
Orthopedic
170d
Cleared
Mar 26, 2021
Toro-L Interbody Fusion System
Orthopedic
171d
Cleared
Dec 03, 2020
LineSider™ Spinal System
Orthopedic
17d
Cleared
Nov 03, 2020
FlareHawk Interbody Fusion System
Orthopedic
90d
Cleared
Sep 23, 2020
FlareHawk TiHawk9 Interbody Fusion System
Orthopedic
124d
Cleared
Jun 21, 2019
LineSider™ Spinal System
Orthopedic
126d
Cleared
Apr 03, 2019
FlareHawk Interbody Fusion System
Orthopedic
135d
Cleared
Jan 07, 2019
FlareHawk Interbody Fusion System
Orthopedic
154d