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 Wuestec Medical with 9 510(k) clearances. The most recent is a 510(k) clearance dated Dec 21, 1999: PENSIL TRAUMA, MODEL WWS6100.
| Dec 21, 1999 | PENSIL TRAUMA, MODEL WWS6100K993962 · KPR | 510(k) clearances |
| Oct 25, 1999 | XRT 600 R/F, WRF 0600K992603 · JAA | 510(k) clearances |
| Sep 1, 1999 | C-QUESTK992103 · OWB | 510(k) clearances |
| Oct 20, 1998 | DX-480, ADD ON DIGITAL IMAGERK981880 · KPR | 510(k) clearances |
| Dec 22, 1997 | LIGHTLINE-MK974240 · IZX | 510(k) clearances |
| Jul 24, 1996 | MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300K960083 · IXQ | 510(k) clearances |
| Jul 24, 1996 | XRT 400K955414 · KXJ | 510(k) clearances |
| Mar 27, 1996 | SUPERSTAND 300K935123 · IYB | 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
