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 13, 2026, FDA's public records list Optus, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Feb 2, 1996: OPTUS OTOSCOPES.
| Date | Record | Source |
|---|---|---|
| Feb 2, 1996 | OPTUS OTOSCOPESK945264 · ERA | 510(k) clearances |
| Jan 22, 1996 | OPTUS ARTHROSCOPE & MINI-ARTHROSCOPE ACCESSORIESK953913 · HRX | 510(k) clearances |
| Dec 21, 1995 | OPTUS BRONCHOSCOPESK945268 · EOQ | 510(k) clearances |
| Sep 12, 1995 | OPTUS HYSTEROSCOPES AND CONTACT HYSTEROSCOPESK945265 · HIH | 510(k) clearances |
| May 26, 1995 | OPTUS CYSTOSCOPES AND PEDIATRIC CYSTOSCOPESK945262 · FAJ | 510(k) clearances |
| May 23, 1995 | OPTUS ARTHROSCOPES AND MINI-ARTHROSCOPESK945267 · HRX | 510(k) clearances |
| Feb 23, 1995 | OPTUS LAPAROSCOPES AND OPERATING LAPAROSCOPESK945266 · GCJ | 510(k) clearances |
| Jan 26, 1995 | OPTUS SINUSCOPES AND ACCESSORIESK944656 · EOB | 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
