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 13, 2026, FDA's public records list TDM Co., Ltd. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Oct 15, 2026: Park's Pectus 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.
| Date | Record | Source |
|---|---|---|
| Oct 15, 2026 | Park's Pectus SystemK263269 · HRS | 510(k) clearances |
| Oct 2, 2026 | TDM Large Bone Plate and Screw SystemK261611 · HRS | 510(k) clearances |
| Oct 1, 2026 | NOVIX Pedicle Screw SystemK263062 · NKB | 510(k) clearances |
| Dec 5, 2024 | TDM Plate and Screw SystemK241128 · HRS | 510(k) clearances |
| Aug 22, 2024 | Femur Reconstruction Interlocking Nail System, Femur Retrograde Interlocking Nail System, Humerus Interlocking Nail System, Tibia Interlocking Nail System, Compression Hip Nail SystemK230071 · HSB | 510(k) clearances |
| Apr 8, 2024 | TDM Anterior Cervical Plate SystemK240423 · KWQ | 510(k) clearances |
| Apr 5, 2024 | TDM Large Bone Plate and Screw SystemK232115 · HRS | 510(k) clearances |
| Jan 18, 2024 | TDM Screw SystemK231860 · HWC | 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
