Expanding Innovations, Inc.
Mountain View, CA, US
Expanding Innovations, Inc. appears in FDA device records in Mountain View, CA. FDA records list 8 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 8 510(k) clearances for Expanding Innovations, Inc. between 2020 and 2025. The busiest year on record is 2025, with 3. The most recent is 2025, with 3.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2020 | 1 |
| 2021 | 1 |
| 2022 | 2 |
| 2023 | 1 |
| 2025 | 3 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K251003 | X-PAC® LLIF Expandable Lateral Cage System | MAX | Substantially Equivalent | |
| K251617 | X-PAC® TLIF Expandable Posterior Cage System; X-PAC® LLIF Expandable Lateral Cage System | MAX | Substantially Equivalent | |
| K250602 | X-PAC® N-GAGE™ Lumbar Plate System | KWQ | Substantially Equivalent | |
| K223174 | X-Pac Expandable LLIF Cage System | MAX | Substantially Equivalent | |
| K222797 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | |
| K220655 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | |
| K203802 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent | |
| K201145 | X-Pac Expandable Lumbar Cage System | MAX | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3007289746 | 3007289746 | Expanding Innovations, Inc. | 110 PIONEER WAY STE I, MOUNTAIN VIEW, CA 94041 US | 2026 | and 1 more, listed in full below |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
- KWQAppliance, Fixation, Spinal Intervertebral Body
- HTFCurette
- GEGElevator, Surgical, General & Plastic Surgery
- HTDForceps
- MAXIntervertebral Fusion Device With Bone Graft, Lumbar
- OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar
- GFJMallet, Surgical, General & Plastic Surgery
- LXHOrthopedic Manual Surgical Instrument
- HTRRasp
- HTXRongeur
- HXGTamp
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain