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 Tissue Technologies with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jul 24, 2000: SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR STRANDS AND….
| Date | Record | Source |
|---|---|---|
| Jul 24, 2000 | SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR STRANDS AND SUTURE HOLESK002071 · FTL | 510(k) clearances |
| May 19, 2000 | SOFTFORM FACIAL IMPLANTK000849 · FTL | 510(k) clearances |
| Sep 22, 1998 | SOFT TISSUE AUGMENTATION YUBE WITH INSERTION TOOLK982475 · FTL | 510(k) clearances |
| Nov 24, 1997 | SOFTFORM FACIAL IMPLANTK973462 · FTL | 510(k) clearances |
| Jun 3, 1997 | TRU-PULSE CO2 SURGICAL LASERK970804 · GEX | 510(k) clearances |
| Feb 12, 1997 | TRU-PULSE LASER (MODIFIED)K963683 · GEX | 510(k) clearances |
| Sep 3, 1996 | SOFT TISSUE AUGMENTATION TUBE (S.T.A.T.)K962496 · FTL | 510(k) clearances |
| Apr 1, 1996 | SOFT TISSUE AUGMENTATION TUBEK960481 · FTL | 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
