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 Microware Precision with 8 510(k) clearances. The most recent is a 510(k) clearance dated Nov 14, 2024: Tandry Q-Locking Plate 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 14, 2024 | Tandry Q-Locking Plate SystemK242814 · HRS | 510(k) clearances |
| Aug 17, 2023 | Tandry Locking Plate SystemK230690 · HRS | 510(k) clearances |
| Nov 10, 2022 | Tandry CMF Plate SystemK220360 · JEY | 510(k) clearances |
| Sep 20, 2022 | Tandry Compression Screw SystemK220359 · HWC | 510(k) clearances |
| Nov 6, 2019 | BIO-RAY A-1 Anchor Screw SystemK182929 · OAT | 510(k) clearances |
| Sep 18, 2018 | Tandry Locking Plate SystemK171904 · HRS | 510(k) clearances |
| May 2, 2012 | MICROWARE BONE PLATES AND BONE SCREWK111008 · HRS | 510(k) clearances |
| Dec 4, 2008 | MICROWARE BONE PLATES AND BONE SCREWSK072562 · 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
