Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in GermanyLabelled 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 Heinz Kurz GmbH with 5 510(k) clearances. The most recent is a 510(k) clearance dated Mar 8, 2001: KURZ ANGULAR PISTON-TITANIUM PROSTHESIS, MODELS 1006 600, 1006 601, 1006 602, 1006 650, ….
| Mar 8, 2001 | KURZ ANGULAR PISTON-TITANIUM PROSTHESIS, MODELS 1006 600, 1006 601, 1006 602, 1006 650, 1006 651, 1006 652K010442 · ETB | 510(k) clearances |
| May 18, 1999 | TITANIUM VOCAL FOLD MEDIALIZING IMPLANT, MODELS 5001 001 (FEMALE), AND 5001 003 (MALE)K991324 · KHJ | 510(k) clearances |
| Mar 31, 1999 | TUBINGEN TITANIUM PROSTHESIS (TTP) VARIO, MODELS AERIAL 1004 010 & BELL 1002 010K990923 · ETB | 510(k) clearances |
| Nov 21, 1997 | K-PISTON WITH BAND HOOK /ANGULAR PISTONK973356 · ETB | 510(k) clearances |
| Aug 4, 1997 | BELL PROSTHESIS (PARTIAL)K972492 · ETB | 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
