Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AlconLabelled 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 Grieshaber & Co. with 15 510(k) clearances. The most recent is a 510(k) clearance dated May 5, 1995: THE GRIESHABER AXIAL CUTTER.
| May 5, 1995 | THE GRIESHABER AXIAL CUTTERK950056 · HKP | 510(k) clearances |
| May 3, 1994 | THE GRIESHABER SYST/AI TUBING SET AND CARTRIDGEK930842 · HQE | 510(k) clearances |
| Jun 11, 1992 | GRIESHABER SNARE INSTRUMENT AND SNARE CARTRIDGEK914588 · GAW | 510(k) clearances |
| Jan 23, 1992 | GRIESHABER AIR/FLUID TUBING SETK914587 · KYG | 510(k) clearances |
| Jan 3, 1992 | GRIESHABER TWO FUNCTION MANIPULATORK914585 · EQH | 510(k) clearances |
| Jan 3, 1992 | GRIESHABER THREE FUNCTION MANIPULATORK914586 · EQH | 510(k) clearances |
| Apr 12, 1990 | GRIESHABER RETINAL TACK AND SUTHERLAND TACK FORCEPK897119 · HQW | 510(k) clearances |
| Mar 27, 1990 | ZZIPP INSTANT BOVIE CLEANERK900714 · GEI | 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
