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 14, 2026, FDA's public records list Medelec, Ltd. and its 1 subsidiaries with 11 510(k) clearances. The most recent is a 510(k) clearance dated Mar 26, 1998: TECA NCS ELECTRODE SYSTEM 2000.
| Mar 26, 1998 | TECA NCS ELECTRODE SYSTEM 2000K971914 · GXY | 510(k) clearances |
| Nov 20, 1997 | TECA MYOJECT DISPOSABLE NEEDLE ELECTRODESK973444 · IKT | 510(k) clearances |
| Nov 20, 1997 | TECA DISPOSABLE MONOPOLAR NEEDLE ELECTRODESK973442 · IKT | 510(k) clearances |
| Jun 20, 1997 | TECA. MILLENNIUMK965065 · GWF | 510(k) clearances |
| Jan 27, 1997 | DG NERVUSK964280 · GWQ | 510(k) clearances |
| Jan 17, 1996 | DG PORTABLE SYSTEMK954157 · OLT | 510(k) clearances |
| Nov 8, 1995 | DG EXAMINER PLUSK953799 · OLT | 510(k) clearances |
| Oct 19, 1995 | TECA PREMIEREK953732 · GWJ | 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
