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 13, 2026, FDA's public records list Teca, Inc. with 29 510(k) clearances. The most recent is a 510(k) clearance dated Dec 16, 1996: EEG ELECTRODES.
| Date | Record | Source |
|---|---|---|
| Dec 16, 1996 | EEG ELECTRODESK962283 · GXY | 510(k) clearances |
| Feb 4, 1991 | SAPPHIRE SERIES 1P, 1L, 2L, AND 2MEK903731 · GWF | 510(k) clearances |
| Nov 15, 1990 | EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPHK903004 · GWQ | 510(k) clearances |
| Feb 16, 1990 | P460, DG32 ELECTROENCEPHALOGRAPHK896666 · GWQ | 510(k) clearances |
| Dec 22, 1989 | TECA NEUROMAPPER 386K894889 · OLT | 510(k) clearances |
| Nov 15, 1989 | TECA NEUROMAPPER 1620, BRAIN MAPPERK894088 · OLT | 510(k) clearances |
| Mar 23, 1989 | TECA 1A96, 1A97 AND 1A98 ELECTROENCEPHALOGRAPHSK890881 · GWQ | 510(k) clearances |
| Feb 23, 1989 | TECA/MEDELEC 'CONCEPT' P420K884870 · GWF | 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
