Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in JapanLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Hoya CorporationLabelled 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 Hoya Conbio with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jun 1, 2009: REVLITE Q-SWITCHED ND:YAG LASER SYSTEM.
| Jun 1, 2009 | REVLITE Q-SWITCHED ND:YAG LASER SYSTEMK083899 · GEX | 510(k) clearances |
| Aug 27, 2008 | SCULPTURE 2.94 ER:YAG SYSTEMK073158 · GEX | 510(k) clearances |
| Feb 14, 2008 | V-RASER DIODE LASER SYSTEMK073332 · GEX | 510(k) clearances |
| Mar 16, 2007 | DIODENT MICRO DENTAL LASER SYSTEM, MODELS 810 AND 980K063384 · GEX | 510(k) clearances |
| Jan 25, 2007 | REVLITE C6 Q-SWITCHED ND:YAG LASER SYSTEMK063834 · GEX | 510(k) clearances |
| Dec 1, 2006 | REVLITE Q-SWITCHED ND:YAG LASERK063112 · GEX | 510(k) clearances |
| May 24, 2006 | MEDLITE C SERIES COMPRESSION TOOL AND HANDPIECE ATTACHMENT ACCESSORY, MODEL 659-0523K060977 · GEX | 510(k) clearances |
| Aug 3, 2004 | VERSAWAVE DENTAL ER:YAG LASER SYSTEMK041710 · GEX | 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
