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 15, 2026, FDA's public records list TTI Medical with 9 510(k) clearances. The most recent is a 510(k) clearance dated May 31, 1995: ACCU-BEAM FIBER OPTIC HANDPIECE.
| May 31, 1995 | ACCU-BEAM FIBER OPTIC HANDPIECEK952006 · GEX | 510(k) clearances |
| May 24, 1995 | ACCU-BEAM 300W XENON LIGHT SOURCEK951895 · GCT | 510(k) clearances |
| Feb 24, 1995 | ACCU-BEAM C02 LASER HANDPIECEK945648 · GEX | 510(k) clearances |
| Jun 1, 1993 | ACCU-BEAM TUBE SETK921208 · GCJ | 510(k) clearances |
| Nov 7, 1991 | ACCU-BEAM LAPAROSCOPIC SYSTEMK910978 · GEI | 510(k) clearances |
| Feb 22, 1990 | ACCU-BEAM WAVEGUIDEK895656 · GEX | 510(k) clearances |
| May 15, 1989 | ACCU-BEAM YAG FIBERK890922 · GEX | 510(k) clearances |
| Mar 9, 1987 | CO2 LASER BRONCHOSCOPE SETK870063 · EOQ | 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
