Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FranceLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Luneau with 5 510(k) clearances. The most recent is a 510(k) clearance dated Apr 24, 2017: VX130 Ophthalmic Diagnostic Device.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Apr 24, 2017 | VX130 Ophthalmic Diagnostic DeviceK162067 · HKX | 510(k) clearances |
| Jun 1, 2015 | VX120 Ophthalmic Diagnostic DeviceK143086 · HKX | 510(k) clearances |
| Feb 20, 2003 | LUNEAU STERILE TONOMETER SEPARATION PRISMSK023838 · HKY | 510(k) clearances |
| Sep 24, 2002 | LUNEAU 3 MIRROR LENSK022413 · HJK | 510(k) clearances |
| May 30, 1985 | ANESTHESIOMETERK851557 · HJC | 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
