FDA applicant

Medelec, Inc. D.B.A. Teca Corp.

Pleasantville, NY3 decisions1997–19980 recalls

FDA records 3 decisions for Medelec, Inc. D.B.A. Teca Corp. (Pleasantville, NY) from 1997 to 1998: 3 510(k) clearances. Most are in product codes IKT (Electrode, Needle, Diagnostic Electromyograph) and GXY (Electrode, Cutaneous). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, physical medicine panel, where it files most

How often FDA has decided Medelec, Inc. D.B.A. Teca Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medelec, Inc. D.B.A. Teca Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medelec, Inc. D.B.A. Teca Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Medelec”

FDA records each applicant name separately; these may or may not be the same firm.

Medelec Intl. Corp. 15 Medelec, Ltd. 8

Medelec, Inc. D.B.A. Teca Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Medelec”