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 Worldwide Medical Technologies with 15 510(k) clearances. The most recent is a 510(k) clearance dated Mar 1, 2007: BRACHYSCIENCES STRANDPORT.
| Mar 1, 2007 | BRACHYSCIENCES STRANDPORTK062214 · KXK | 510(k) clearances |
| Jul 2, 2003 | READI-STRAND, MODEL PSSTRANDK023179 · KXK | 510(k) clearances |
| Jun 9, 2003 | READI-STRAND, MODEL PSSTRANDK022705 · KXK | 510(k) clearances |
| May 6, 2003 | READI-LOAD SYSTEM, MODEL PSS 1820RLK022389 · KXK | 510(k) clearances |
| Oct 29, 2002 | SPIRITUS(TM) RESPIRATORY SYSTEM #SRS 001K020641 · BZD | 510(k) clearances |
| Jul 29, 2002 | READI-STRAND; MODEL PSSTRANDK020337 · KXK | 510(k) clearances |
| May 20, 2002 | BONE MARROW ASPIRATION NEEDLE, MODEL BMB1110J, BONE MARROW HARVEST NEEDLE, MODEL BMHN1104VX, & BONE MARROW BIOPSY NEEDLK020867 · KNW | 510(k) clearances |
| Nov 5, 1999 | WORLDWIDE MEDICAL TECHNOLOGIES SEEDING SPACERSK991344 · KXK | 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
