Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Meditech Spine with 10 510(k) clearances. The most recent is a 510(k) clearance dated Mar 18, 2021: Cure 2.0 Anterior Cervical Plate (ACP) System.
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.
| Mar 18, 2021 | Cure 2.0 Anterior Cervical Plate (ACP) SystemK210286 · KWQ | 510(k) clearances |
| Sep 11, 2020 | Talos®-C Cervical Intervertebral Body Fusion System, Talos®-C (HA) Cervical Intervertebral Body Fusion SystemK201506 · ODP | 510(k) clearances |
| May 12, 2020 | Cure™ Lumbar Plate SystemK201136 · KWQ | 510(k) clearances |
| Aug 31, 2018 | Cure™ OPEL-C Plate SystemK181543 · KWQ | 510(k) clearances |
| Apr 23, 2018 | Cure™ Lumbar Plate SystemK180090 · KWQ | 510(k) clearances |
| Jun 16, 2017 | Cure™ Lumbar Plate SystemK171538 · KWQ | 510(k) clearances |
| Jun 2, 2017 | Talos® Lumbar (HA) PEEK IBF DevicesK170395 · MAX | 510(k) clearances |
| Jul 1, 2016 | Cure™ Anterior Cervical Plate (ACP) SystemK160604 · KWQ | 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
