Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of LivaNovaLabelled 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 Stoeckert Instrumente with 13 510(k) clearances. The most recent is a 510(k) clearance dated Jan 29, 2001: STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAE.
| Jan 29, 2001 | STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAEK002273 · DWF | 510(k) clearances |
| Jan 25, 2001 | STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAEK001961 · DWF | 510(k) clearances |
| Aug 9, 2000 | STOCKERT COMPACT SYSTEM VERSION 2.0K002118 · DTQ | 510(k) clearances |
| Dec 20, 1999 | INTERFACE MODULE IDDDK992635 · KRI | 510(k) clearances |
| Nov 23, 1999 | STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTSK990512 · KRI | 510(k) clearances |
| Sep 4, 1998 | STOCKERT COMPACT SYSTEMK982014 · DTQ | 510(k) clearances |
| Feb 27, 1998 | S3 MAST PUMPK972321 · DWB | 510(k) clearances |
| Sep 10, 1997 | S3 CYCLIC RPM CONTROLK971520 · DWB | 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
