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., 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 Howmedica Leibinger, Inc. with 11 510(k) clearances. The most recent is a 510(k) clearance dated Oct 1, 1997: LEIBINGER SELF-DRILLING SCREW.
| Oct 1, 1997 | LEIBINGER SELF-DRILLING SCREWK970912 · HWC | 510(k) clearances |
| Aug 11, 1997 | COHEN DISTRACTORK972154 · JEY | 510(k) clearances |
| Aug 11, 1997 | GUERRERO - BELL DISTRACTORK972166 · JEY | 510(k) clearances |
| Jul 17, 1997 | EPITEC TITANIUM IMPLANT SYSTEM FOR THE SURGICAL ANCHORING OF FACIAL PROSTHESESK961719 · HRS | 510(k) clearances |
| Apr 11, 1997 | LEIBINGER IMF SCREWK963030 · DZE | 510(k) clearances |
| Apr 11, 1997 | LEE PLATEK970911 · JEY | 510(k) clearances |
| Feb 6, 1997 | LEIBINGER LUHR SMALL CRANIOMAXILLOFACIAL BONE SCREWSK963741 · HRS | 510(k) clearances |
| Jan 24, 1997 | VAZQUEZ DINER INTRAORAL DISTRACTION DEVICEK964649 · JEY | 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
