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 Wiltrom Corporation Limited with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 23, 2020: Wiltrom Spinal Fixation 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 23, 2020 | Wiltrom Spinal Fixation SystemK202894 · NKB | 510(k) clearances |
| Oct 24, 2018 | Osteocera Resorbable Bone SubstituteK180758 · MQV | 510(k) clearances |
| Feb 2, 2018 | Bicera Resorbable Bone SubstituteK172237 · MQV | 510(k) clearances |
| Jan 12, 2018 | Wiltrom Spinal Fixation SystemK172548 · NKB | 510(k) clearances |
| Sep 18, 2012 | BICERA (TM) RESORBABLE BONE SUBSTITUTEK110949 · MQV | 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
