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 Biodynamic Technologies, Inc. with 30 510(k) clearances. The most recent is a 510(k) clearance dated Mar 31, 1999: ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEM.
| Date | Record | Source |
|---|---|---|
| Mar 31, 1999 | ULTIMAX TROCHANTERIC INTRAMEDULLARY ROD SYSTEMK990436 · HSB | 510(k) clearances |
| Mar 17, 1999 | ULTIMAX DISTAL RADIAL (VOLAR) LOCKING PLATE SYSTEMK990481 · HRS | 510(k) clearances |
| Mar 17, 1999 | ULTIMAX CORTICAL BONE SCREWSK990513 · HWC | 510(k) clearances |
| Jun 1, 1998 | ULTIMAX DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEMK981230 · HSB | 510(k) clearances |
| Apr 3, 1998 | BTI HUMERAL INTRAMEDULLARY ROD SYSTEMK980102 · HSB | 510(k) clearances |
| Mar 12, 1998 | BTI LARGE (7.0MM) CANNULATED TRANSFIXING SCREWSK974756 · HWC | 510(k) clearances |
| Aug 29, 1997 | BTI CORTICAL BONE SCREWSK972403 · HWC | 510(k) clearances |
| Apr 21, 1997 | BTI DISTAL FEMORAL INTRAMEDULLARY ROD SYSTEMK970897 · HSB | 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
