Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled 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 14, 2026, FDA's public records list Ophthalmic Technologies with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jan 21, 2005: OCT-OPTHALMOSCOPE.
| Jan 21, 2005 | OCT-OPTHALMOSCOPEK042885 · HLI | 510(k) clearances |
| Jun 20, 2003 | HF MODULE WITH TRANSDUCERSK031391 · IYO | 510(k) clearances |
| Mar 27, 2003 | OTI SCAN WITH TRANSDUCERSK030770 · IYO | 510(k) clearances |
| Jan 10, 2003 | A-SCAN 100K024114 · IYO | 510(k) clearances |
| Apr 4, 1999 | DI-RHEX OPHTHALMIC DIATHERMY SYSTEMK990064 · HQR | 510(k) clearances |
| Feb 25, 1998 | 3D I-SCANK974522 · IYO | 510(k) clearances |
| Jun 25, 1997 | I-SCOPE OPHTHALMIC ENDOSCOPEK971679 · MPA | 510(k) clearances |
| May 13, 1996 | I-SCANK960622 · IYO | 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
