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 Carl Zeiss MeditecLabelled 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 Zeiss Humphrey Systems with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 1, 1994: ZEISS OPMILAS 144 SURGICAL LASERS.
| Jul 1, 1994 | ZEISS OPMILAS 144 SURGICAL LASERSK942439 · GEX | 510(k) clearances |
| Nov 8, 1993 | DIGITAL OPHTHALMIC ULTRASOUND BIOMICROSCOPEK923211 · IYO | 510(k) clearances |
| Dec 10, 1992 | OPHTHALMIC A/B SCAN SYSTEM, MODEL 835 -- MODIFIEDK923348 · ITX | 510(k) clearances |
| Sep 18, 1985 | HUMPHREY FIELD ANALYZER MODEL 630K852639 · HPT | 510(k) clearances |
| Aug 12, 1985 | HUMPHREY IMAGE ANALYZER MODEL 110K852638 · HKI | 510(k) clearances |
| Jul 28, 1982 | THE HUMPHREY FIELD ANALYZER MODEL 610K821940 · HPT | 510(k) clearances |
| Nov 12, 1980 | OBJECTIVE REFRACTORK802029 · HKO | 510(k) clearances |
| Feb 12, 1979 | AUTOKERATOMETER, INSTRUMENTK781994 · HLQ | 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
