Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Theramicro with 5 510(k) clearances. The most recent is a 510(k) clearance dated Oct 21, 2026: TeKBrace Knotless Anchor.
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.
| Oct 21, 2026 | TeKBrace Knotless AnchorK263352 · MBI | 510(k) clearances |
| Aug 18, 2026 | TeKBrace Solo Soft Tissue Reinforcement DeviceK262729 · QUW | 510(k) clearances |
| Jun 9, 2026 | TekBrace Solo Soft Tissue Reinforcement DeviceK261621 · QUW | 510(k) clearances |
| Mar 6, 2026 | TeKBrace Knotless AnchorK253538 · MBI | 510(k) clearances |
| May 30, 2025 | TekBrace Solo Soft Tissue Reinforcement DeviceK251063 · QUW | 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
