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.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Luxtec Corp. with 15 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 1997: LUXSCOPE.
| Date | Record | Source |
|---|---|---|
| Nov 21, 1997 | LUXSCOPEK973193 · HQF | 510(k) clearances |
| May 21, 1997 | TENOSCOPEK970642 · HRX | 510(k) clearances |
| May 14, 1997 | TENOSNAREK970562 · HRX | 510(k) clearances |
| Sep 8, 1995 | REDDY ILLUMINATORK950960 · FFS | 510(k) clearances |
| Sep 15, 1989 | IMS5000 ILLUMINATED LOUPESK895248 · FSP | 510(k) clearances |
| Apr 26, 1989 | LUXTEC ACO SERIES 4000 LIGHT SOURCEK890716 · FCW | 510(k) clearances |
| May 22, 1987 | LUXTEC FIBEROPTIC CABLESK864387 · EQH | 510(k) clearances |
| Jan 14, 1987 | FRAZIER SUCTION TUBEK864382 · EQH | 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
