Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Miami Device Solutions with 7 510(k) clearances and 1 device recall. The most recent is a device recall dated Jan 15, 2019: Proximal Humerus Plate, 8 holes, Right, REF MDS130108R - Product Usage: The Proximal Hum….
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.
| Jan 15, 2019 | Proximal Humerus Plate, 8 holes, Right, REF MDS130108R - Product Usage: The Proximal Humerus Plating System consists of plates, screws, and Class II · Right Proximal Humerus Plates. Product component parts MDS130108R, may be improperly identified as left. | Device recalls |
| Dec 10, 2018 | Distal Radius Plating SystemK182810 · HRS | 510(k) clearances |
| Dec 8, 2017 | MDS Plating SystemK172786 · HRS | 510(k) clearances |
| Mar 17, 2017 | Olecranon Plating SystemK162898 · HRS | 510(k) clearances |
| Oct 21, 2016 | Distal Radius Plating SystemK162635 · HRS | 510(k) clearances |
| Aug 15, 2016 | Distal Radius Plating SystemK161292 · HRS | 510(k) clearances |
| Jul 29, 2016 | Cannulated ScrewK161058 · HWC | 510(k) clearances |
| Mar 20, 2015 | PROXIMAL HUMERUS PLATING SYSTEMK141493 · HRS | 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
