Consumer health companyLabelled 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 Truemed Group, LLC with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 9, 2021: TRUEMED HAND, FOOT AND ANKLE PLATES 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.
| Jul 9, 2021 | TRUEMED HAND, FOOT AND ANKLE PLATES SYSTEMK200575 · HRS | 510(k) clearances |
| Jun 10, 2019 | Arzzt Distal Radius and Ulna SystemK182650 · HRS | 510(k) clearances |
| Jan 16, 2018 | Ins Hilden Humeral Arzzt, Ins Hilden Cannulated Tibial Arzzt, Ins Hilden Femoral Arzzt & Ins Hilden Retrograde Femoral ArzztK172189 · HSB | 510(k) clearances |
| Aug 3, 2017 | Arzzt 3.5 / 4.5 Small & Large Fragments SystemK162507 · HRS | 510(k) clearances |
| Nov 6, 2014 | INS HILDEN TIBIAL ARZZTK133166 · 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
