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., part of TeleflexLabelled by claude-sonnet-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 Edward Weck with 140 510(k) clearances. The most recent is a 510(k) clearance dated Jun 29, 1992: WECK TROCAR.
| Jun 29, 1992 | WECK TROCARK915378 · HET | 510(k) clearances |
| Mar 23, 1992 | LM15(TM), CATALOG NUMBER - 523821K914690 · GCJ | 510(k) clearances |
| Jan 9, 1992 | HEMOCLIP IIK911915 · FZP | 510(k) clearances |
| Nov 29, 1991 | PNEUMO-SEAL(TM)K914470 · GCJ | 510(k) clearances |
| Jul 2, 1991 | ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705K911272 · FHG | 510(k) clearances |
| Aug 6, 1990 | HEM-O-LOK(TM)K902108 · FZP | 510(k) clearances |
| Aug 2, 1990 | WECK ELECTROSURGICAL GENERATOR #174200K902232 · GEI | 510(k) clearances |
| Feb 15, 1990 | BOWIE-DICK TEST CARD CATALOG NUMBER 008018K897045 · JOJ | 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
