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 Teknomed, Inc. with 7 510(k) clearances. The most recent is a 510(k) clearance dated May 21, 1993: TECHNOMED PULSOLITH 4000 LASER SYSTEM.
| May 21, 1993 | TECHNOMED PULSOLITH 4000 LASER SYSTEMK925395 · LNK | 510(k) clearances |
| Nov 5, 1992 | MULTILASE 2100 C, 2100 DK913917 · GEX | 510(k) clearances |
| Nov 5, 1992 | MULTILASE 2500 AK920708 · GEX | 510(k) clearances |
| Feb 21, 1992 | MULTILASE 2100 AK913290 · GEX | 510(k) clearances |
| Oct 6, 1989 | TECHNOMED PULSOLITH LASER SYSTEMK895178 · FFK | 510(k) clearances |
| Mar 23, 1989 | TECHNOMED PULSOLITH LASER SYSTEMK890436 · FFK | 510(k) clearances |
| Feb 21, 1979 | TECNOTOMOK790132 · IZF | 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
