Medical device makerLabelled 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 13, 2026, FDA's public records list Laserguide with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 22, 1988: SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE.
| Date | Record | Source |
|---|---|---|
| Mar 22, 1988 | SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USEK880071 · FCS | 510(k) clearances |
| Feb 2, 1988 | SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USEK873892 · LNK | 510(k) clearances |
| Feb 2, 1988 | SURGI-LIGHT DISPOSABLE SYSTEM FOR PULMONOLOGY USEK875104 · LLO | 510(k) clearances |
| Nov 6, 1987 | LIGHT-SPOT FIBEROPTIC LASER HANDPIECEK873664 · GEX | 510(k) clearances |
| Nov 6, 1987 | LIGHT-TOUCH FIBEROPTIC MICROCONTACT PROBEK873571 · 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
