Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in IrelandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of StrykerLabelled 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 15, 2026, FDA's public records list Stryker Ireland Ltd. with 2 510(k) clearances. The most recent is a 510(k) clearance dated Dec 29, 2008: STRYKER DISPOSABLE CRANIAL PERFORATOR BIT.
| Dec 29, 2008 | STRYKER DISPOSABLE CRANIAL PERFORATOR BITK082010 · HBF | 510(k) clearances |
| Aug 26, 2008 | STRYKER ESSX MICRODEBRIDER SYSTEMK073633 · ERL | 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
