Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of TeleflexLabelled 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 Rusch International with 43 510(k) clearances. The most recent is a 510(k) clearance dated Dec 23, 2003: INTERMITTENT URETHRAL CATHETERS.
| Dec 23, 2003 | INTERMITTENT URETHRAL CATHETERSK033023 · KOD | 510(k) clearances |
| Jun 30, 2003 | RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEMK030559 · ESW | 510(k) clearances |
| Jun 17, 2003 | RUSCH GUIDED CHOLANGIOGRAPHY CATHETERK023666 · FGE | 510(k) clearances |
| Mar 28, 2003 | RUSCH CRYSTAL CLEAR TRACHEOSTOMY SETS, CUFFED AND CUFFLESSK023918 · JOH | 510(k) clearances |
| Dec 23, 2002 | RUSCH MICROLARYNGEAL TUBEK023964 · BTR | 510(k) clearances |
| Aug 1, 2002 | RUSCH EDGAR TUBEK021540 · BTR | 510(k) clearances |
| Jul 23, 2002 | RUSCH TRACHEOFIX SET, CUFFED AND UNCUFFEDK021764 · BTO | 510(k) clearances |
| Jul 1, 2002 | RUSCH FLONEIL; FLOCATH INTROGELK020714 · GBM | 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
