Medical Device Manufacturer · US , Jupiter , FL

Integrity Implants, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 2019
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.

FDA 510(k) cleared devices by Integrity Implants, Inc.

11 devices
1-11 of 11
Cleared Aug 07, 2023
LineSider® Spinal System
K231098 · NKB
Orthopedic · 111d
Cleared Mar 25, 2022
Toro-L Interbody Fusion System
K213355 · MAX
Orthopedic · 164d
Cleared Mar 24, 2022
FlareHawk Interbody Fusion System
K220453 · MAX
Orthopedic · 35d
Cleared Dec 23, 2021
Integrity Implants Navigated Instruments
K212088 · OLO
Orthopedic · 170d
Cleared Mar 26, 2021
Toro-L Interbody Fusion System
K203038 · MAX
Orthopedic · 171d
Cleared Dec 03, 2020
LineSider™ Spinal System
K203367 · NKB
Orthopedic · 17d
Cleared Nov 03, 2020
FlareHawk Interbody Fusion System
K202198 · MAX
Orthopedic · 90d
Cleared Sep 23, 2020
FlareHawk TiHawk9 Interbody Fusion System
K201367 · MAX
Orthopedic · 124d
Cleared Jun 21, 2019
LineSider™ Spinal System
K190360 · NKB
Orthopedic · 126d
Cleared Apr 03, 2019
FlareHawk Interbody Fusion System
K183184 · MAX
Orthopedic · 135d
Cleared Jan 07, 2019
FlareHawk Interbody Fusion System
K182114 · MAX
Orthopedic · 154d
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