Medical device makerLabelled 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 M. Imonti and Associates Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated May 22, 1995: PRO-PAK FOR OMS DIPLOMATE.
| May 22, 1995 | PRO-PAK FOR OMS DIPLOMATEK950800 · HQC | 510(k) clearances |
| Apr 28, 1995 | PRO-VITK950799 · HQE | 510(k) clearances |
| Jan 25, 1994 | PHACOFRAGMENTOR TIPK933627 · HQC | 510(k) clearances |
| Jan 6, 1994 | PRO-PHACO HANDPIECEK933503 · HQC | 510(k) clearances |
| Dec 8, 1992 | ENDO TRACHEA TUBE FIXATIONK924551 · CBH | 510(k) clearances |
| Mar 6, 1991 | DRAINAGE TUBE RESTRAINT/WOUND COVERK905766 · GBX | 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
