Expanding Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Expanding Innovations, Inc. - FDA 510(k) Cleared Devices
Recent clearances: X-PAC® LLIF Expandable Lateral Cage System, X-PAC® TLIF Expandable Posterior Cage System, X-PAC® N-GAGE™ Lumbar Plate System
8
Total
8
Cleared
0
Denied
Expanding Innovations, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mountain View, US.
Latest FDA clearance: Jun 2025. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Expanding Innovations, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Kapstone Medical, LLC, Helix Medical, LLC and Lince Consulting, LLC.
FDA 510(k) Regulatory Record - Expanding Innovations, Inc.
8 devices
Cleared
Jun 25, 2025
X-PAC® LLIF Expandable Lateral Cage System
Orthopedic
85d
Cleared
Jun 16, 2025
X-PAC® TLIF Expandable Posterior Cage System
Orthopedic
20d
Cleared
May 20, 2025
X-PAC® N-GAGE™ Lumbar Plate System
Orthopedic
81d
Cleared
Feb 14, 2023
X-Pac Expandable LLIF Cage System
Orthopedic
126d
Cleared
Oct 14, 2022
X-Pac Expandable Lumbar Cage System
Orthopedic
28d
Cleared
Mar 24, 2022
X-Pac Expandable Lumbar Cage System
Orthopedic
17d
Cleared
Jun 07, 2021
X-Pac Expandable Lumbar Cage System
Orthopedic
161d
Cleared
Sep 10, 2020
X-Pac Expandable Lumbar Cage System
Orthopedic
134d