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

- Location (FDA's records): Pleasantville, NY
- FDA decisions: 3 (1997–1998): 3 510(k) clearances
- Product codes: IKT (2), GXY (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 10 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Technomed Europe: 2 (https://510kreport.com/company/technomed-europe)
- Spes Medica Srl: 2 (https://510kreport.com/company/spes-medica)
- Natus Manufacturing Limited: 2 (https://510kreport.com/company/natus-manufacturing)
- Axon Systems, Inc.: 1 (https://510kreport.com/company/axon-systems)
- Ambu A/S: 1 (https://510kreport.com/company/ambu-a-s)
- Medtronic Xomed, Inc.: 1 (https://510kreport.com/company/medtronic-xomed)
- Vertis Neuroscience, Inc.: 1 (https://510kreport.com/company/vertis-neuroscience)

## Its most-cited devices
- K973444: Teca Myoject Disposable Needle Electrodes (1997), cited by 6
- K971914: Teca NCS Electrode System 2000 (1998), cited by 2
- K973442: Teca Disposable Monopolar Needle Electrodes (1997), cited by 2

## Recent decisions
- K971914: Teca NCS Electrode System 2000 (Mar 26, 1998)
- K973442: Teca Disposable Monopolar Needle Electrodes (Nov 20, 1997)
- K973444: Teca Myoject Disposable Needle Electrodes (Nov 20, 1997)

Source page: https://510kreport.com/company/medelec-dba-teca