Data / Medical devices / United States / Expanding Innovations, Inc.
Expanding Innovations, Inc.: FDA-registered device maker in Mountain View, CA, United States, 9 510(k) clearances
Expanding Innovations, Inc. is registered with the FDA (registration 3007289746) in Mountain View, CA, United States. It lists 11 device types. The FDA files 9 510(k) clearances under its listings, the newest dated June 16, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3007289746
- Address
- 110 Pioneer Way Ste I, Mountain View, CA, United States, 94041
- Owner or operator
- EXPANDING INNOVATIONS INC (10058298)
- Roles
- Complaint file establishment, Manufacturer
- First device listed
- August 17, 2018
- Registered through
- 2026
- Brand names listed
- Bayonet Cup Curette, Rasp, X-PAC, X-PAC N-GAGE Lumbar Plate System, X-Pac, X-Pac Expandable Cage System, X-Pac Strike Cap, cobb and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Appliance, Fixation, Spinal Intervertebral Body | KWQ | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Curette | HTF | 1 | Complaint file establishment | accessdata.fda.gov |
| Elevator, Surgical, General & Plastic Surgery | GEG | 1 | Complaint file establishment | accessdata.fda.gov |
| Forceps | HTD | 1 | Complaint file establishment | accessdata.fda.gov |
| Intervertebral Fusion Device With Bone Graft, Lumbar | MAX | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Intervertebral Fusion Device With Integrated Fixation, Lumbar | OVD | 2 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Mallet, Surgical, General & Plastic Surgery | GFJ | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Orthopedic Manual Surgical Instrument | LXH | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
| Rasp | HTR | 1 | Complaint file establishment | accessdata.fda.gov |
| Rongeur | HTX | 1 | Complaint file establishment | accessdata.fda.gov |
| Tamp | HXG | 1 | Complaint file establishment, Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| June 16, 2025 | K251617 | X-PAC® TLIF Expandable Posterior Cage System; X-PAC® LLIF Expandable Lateral Cage System | MAX | Substantially Equivalent | Expanding Innovations, Inc. | accessdata.fda.gov |
| May 20, 2025 | K250602 | X-PAC® N-GAGE Lumbar Plate System | KWQ | Substantially Equivalent | Expanding Innovations, Inc. | accessdata.fda.gov |
| February 14, 2023 | K223174 | X-Pac Expandable LLIF Cage System | MAX | Substantially Equivalent | Expanding Innovations, Inc. | accessdata.fda.gov |
| October 14, 2022 | K222797 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | Expanding Innovations, Inc. | accessdata.fda.gov |
| March 24, 2022 | K220655 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | Expanding Innovations, Inc. | accessdata.fda.gov |
| June 7, 2021 | K203802 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | Expanding Innovations, Inc. | accessdata.fda.gov |
| September 10, 2020 | K201145 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | Expanding Innovations, Inc. | accessdata.fda.gov |
| August 1, 2016 | K160856 | SpineView X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | Spine View, Inc. | accessdata.fda.gov |
| February 24, 2016 | K152539 | SpineView X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | Spine View, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Intervertebral Fusion Device With Bone Graft, Lumbar
- All makers of Rasp
- All makers of Tamp
- All makers of Elevator, Surgical, General & Plastic Surgery
- All makers of Mallet, Surgical, General & Plastic Surgery
- All makers of Rongeur
Updated June 16, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.