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 14, 2026, FDA's public records list Laser Media with 12 510(k) clearances. The most recent is a 510(k) clearance dated Dec 30, 1987: FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA.
| Dec 30, 1987 | FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIAK872352 · HHR | 510(k) clearances |
| Dec 11, 1987 | FIBERLASE II ND:YAG LASER FOR PULMONARY USEK872351 · LLO | 510(k) clearances |
| Aug 10, 1987 | FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USEK872350 · LNK | 510(k) clearances |
| Aug 4, 1987 | UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEMK872031 · LNK | 510(k) clearances |
| Dec 3, 1986 | SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAGK863428 · LNK | 510(k) clearances |
| Nov 24, 1986 | CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASERK863583 · LNK | 510(k) clearances |
| Sep 25, 1986 | FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIAK862444 · HHR | 510(k) clearances |
| Feb 5, 1986 | ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEMK860063 · LNK | 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
