Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Zimmer BiometLabelled by claude-sonnet-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 Core-Vent Corp. with 25 510(k) clearances. The most recent is a 510(k) clearance dated Dec 8, 2000: ADVENT IMPLANT SYSTEM.
| Dec 8, 2000 | ADVENT IMPLANT SYSTEMK002614 · DZE | 510(k) clearances |
| Oct 30, 2000 | SWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, SPB 8,10,12,14/OP3.5D/OPAR,OPB 8,10,12,14/OP2.3D/OP2.8D,K002188 · DZE | 510(k) clearances |
| Jul 11, 1995 | SCREW-VENT IMPLANTK950578 · DZE | 510(k) clearances |
| Jul 11, 1995 | BIO-VENT X IMPLANTK950576 · DZE | 510(k) clearances |
| Jul 11, 1995 | MICRO-VENT IMPLANTK950579 · DZE | 510(k) clearances |
| Jul 11, 1995 | SWEDE-VENT IMPLANTK950577 · DZE | 510(k) clearances |
| Jul 11, 1995 | BIO-VENT IMPLANTK950575 · DZE | 510(k) clearances |
| Feb 11, 1992 | PRE-ANGLED ABUTMENTSK912059 · 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
