Medical device makerLabelled 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 Embody, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 19, 2025: Tapestry Biointegrative Implant.
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.
| Sep 19, 2025 | Tapestry Biointegrative ImplantK252647 · OWY | 510(k) clearances |
| Jun 2, 2023 | ACTIVBRAID™K223822 · GAT | 510(k) clearances |
| May 23, 2022 | Tapestry Biointegrative ImplantK220867 · OWY | 510(k) clearances |
| Apr 8, 2022 | Bioabsorbable AnchorK213958 · MAI | 510(k) clearances |
| Nov 2, 2021 | Tapestry Biointegrative ImplantK212306 · OWY | 510(k) clearances |
| Oct 19, 2020 | TAPESTRY Biointegrative ImplantK201572 · OWY | 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
