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 15, 2026, FDA's public records list Sulzer Dental with 9 510(k) clearances. The most recent is a 510(k) clearance dated Nov 13, 2002: HEX-LOCK TEMPORARY ABUTMENT.
| Nov 13, 2002 | HEX-LOCK TEMPORARY ABUTMENTK014050 · DZE | 510(k) clearances |
| Mar 20, 2002 | SULZER DENTAL CERAMIC SYSTEM-HEXLOCKK014175 · NHA | 510(k) clearances |
| Mar 19, 2002 | SULZER DENTAL CERAMIC SYSTEM-SPLINEK014214 · DZE | 510(k) clearances |
| Jan 18, 2002 | 3.75MM AND 5.0MM SPLINE TWIST IMPLANTK013494 · DZE | 510(k) clearances |
| Nov 19, 2001 | SCREW VENT IMPLANT; TAPERED SCREW VENT IMPLANTK013227 · DZE | 510(k) clearances |
| Sep 6, 2001 | 3.25MM SPLINE TWIST IMPLANTK012055 · DZE | 510(k) clearances |
| Jun 25, 2001 | ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEMK011245 · DZE | 510(k) clearances |
| May 21, 2001 | SCREW-VENT DENTAL IMPLANT SYSTEMK011028 · DZE | 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
