Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list 4Web, Inc. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Feb 12, 2026: Lumbar Spine Truss System - Plating Solution (LSTS-PS).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Feb 12, 2026 | Lumbar Spine Truss System - Plating Solution (LSTS-PS)K253201 · KWQ | 510(k) clearances |
| Mar 10, 2021 | Lumbar Spine Truss System Plating Solution (LSTS-PS)K203065 · KWQ | 510(k) clearances |
| May 29, 2020 | Anterior Spine Truss System – Stand Alone (ASTS-SA) Interbody Fusion DeviceK200002 · OVD | 510(k) clearances |
| Aug 12, 2019 | Cervical Spinal Truss System-Stand Alone (CSTS-SA)K190870 · OVE | 510(k) clearances |
| Jul 23, 2019 | Hammertoe Truss System (HTS)K190926 · HTY | 510(k) clearances |
| Feb 22, 2018 | Osteotomy Truss System (OTS)K172294 · HRS | 510(k) clearances |
| Jan 8, 2018 | Cervical Spinal Truss System (CSTS) Interbody Fusion DeviceK173159 · ODP | 510(k) clearances |
| Nov 7, 2017 | Lateral Spinal Truss System (LSTS) Interbody Fusion DeviceK172392 · MAX | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
