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., part of GetingeLabelled 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 Stierlen-Maquet AG with 10 510(k) clearances. The most recent is a 510(k) clearance dated Mar 14, 1997: MOBILE OPERATING TABLE 1132.01.
| Mar 14, 1997 | MOBILE OPERATING TABLE 1132.01K970807 · GDC | 510(k) clearances |
| Oct 12, 1993 | BETASTAR 1131.02 MOBILE OPERATING TABLEK926525 · FQO | 510(k) clearances |
| Jul 2, 1992 | OPERATING TABLE SYSTEM-BETAMAQUET 1140K920890 · FQO | 510(k) clearances |
| Sep 15, 1988 | OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.K883613 · GDC | 510(k) clearances |
| Sep 17, 1987 | PLASTER TABLE 1418K873274 · JEB | 510(k) clearances |
| Sep 17, 1987 | EXTENSION TABLE 1417K873275 · JEB | 510(k) clearances |
| Sep 17, 1987 | ORTHOPAEDIC TABLE 1420K873273 · JEB | 510(k) clearances |
| Sep 17, 1987 | EXTENSION DEVICE 1416K873276 · JEB | 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
