Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of AbbVie. FDA records under its name, each linked to the record. See the AbbVie group view.
As of Nov 15, 2026, FDA's public records list Allergan Humphrey with 3 510(k) clearances. The most recent is a 510(k) clearance dated Aug 14, 1990: ALLERGAN HUMPHREY A/B SCAN , MODEL 835.
| Aug 14, 1990 | ALLERGAN HUMPHREY A/B SCAN , MODEL 835K902582 · IYO | 510(k) clearances |
| Jul 15, 1987 | MODEL 3000 OPHTHALMIC SURGICAL SYSTEMK872312 · HQE | 510(k) clearances |
| May 18, 1987 | ALLERGAN HUMPHREY AUTO-REFRACTOR, MODELS 525 & 540K871611 · HKO | 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
