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 ElektaLabelled 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 14, 2026, FDA's public records list Elekta Instruments, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jan 15, 1999: ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLE.
| Jan 15, 1999 | ELEKTA ONCOLOGY SYSTEMS PRECISE TREATMENT TABLEK983678 · JAI | 510(k) clearances |
| Oct 17, 1996 | SPETZLER TI 100 ANEURYSM CLIPK955064 · HCH | 510(k) clearances |
| Mar 22, 1996 | LEKSELL NEURO GENERATOR AND ACCESSORIESK941823 · GXD | 510(k) clearances |
| May 23, 1995 | CMF-TITANIUM CRANIO-MAXILLO-FACIAL FRACTURE FIXATION (OSTEOSYNTHESIS) SYSTEMK946165 · HRS | 510(k) clearances |
| Jan 20, 1995 | LEKSELL SURGIPLANK943468 · HAW | 510(k) clearances |
| Jan 7, 1994 | ES-100 ACCESSORIESK932261 · HWE | 510(k) clearances |
| Sep 7, 1993 | ES-100 POWER SYSTEM, ES-100 SERIESK925360 · GEY | 510(k) clearances |
| Jan 23, 1992 | LEKSELL GAMMAPLAN (LGP)K914808 · IWB | 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
