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 Endo InternationalLabelled 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 Laserscope with 60 510(k) clearances. The most recent is a 510(k) clearance dated Dec 1, 2006: GREENLIGHT HPS SERIES SURGICAL LASER SYSTEM & ACCESSORIES.
| Dec 1, 2006 | GREENLIGHT HPS SERIES SURGICAL LASER SYSTEM & ACCESSORIESK062719 · GEX | 510(k) clearances |
| Jun 27, 2006 | LASERSCOPE GUIDED DELIVERY DEVICE (GDD) CYSTOURETHROSCOPE & ACCESSORIESK061646 · FBO | 510(k) clearances |
| Mar 30, 2004 | GEMINI SURGICAL LASER SYSTEM & ACCESSORIESK034011 · GEX | 510(k) clearances |
| Nov 17, 2003 | AURA ISURGICAL LASER SYSTEM & ACCESSORIESK024206 · GEX | 510(k) clearances |
| Jul 2, 2002 | LYRA SURGICAL LASER SYSTEM AND ACCESSIORIES (ND:YAG CONFIGURATION)K020021 · GEX | 510(k) clearances |
| May 21, 2001 | LYRA SERIES SURGICAL LASER SYSTEM & ACCESSORIESK010834 · GEX | 510(k) clearances |
| May 1, 2001 | LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION)K010284 · GEX | 510(k) clearances |
| Mar 6, 2001 | LYRA G SERIES SURGICAL LASER SYSTEM (SL SERIES Q-SWITCHED ND:YAG CONFIGURATION)K003765 · 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
