Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled 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 15, 2026, FDA's public records list Double Medical Technology with 12 510(k) clearances. The most recent is a 510(k) clearance dated Nov 18, 2025: Universal Spinal 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.
| Nov 18, 2025 | Universal Spinal SystemK252729 · NKB | 510(k) clearances |
| Dec 4, 2024 | Locking Screw,CoCrMoK242348 · HWC | 510(k) clearances |
| Nov 22, 2023 | Posterior Cervical Spine SystemK233078 · NKG | 510(k) clearances |
| Mar 14, 2023 | Cervical Plate SystemK223753 · KWQ | 510(k) clearances |
| Jan 25, 2023 | Advanced Bone PlateK221150 · HRS | 510(k) clearances |
| Jan 18, 2023 | Anatomic Bone PlateK221088 · HRS | 510(k) clearances |
| Jan 10, 2023 | Metal Cannulated ScrewK221090 · HWC | 510(k) clearances |
| Dec 21, 2022 | Advanced Intramedullary Nail SystemK221221 · HSB | 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
