Medelec, Inc. D.B.A. Teca Corp.
United StatesFDA applicant, unverified
- Devices
- 3
What Medelec, Inc. D.B.A. Teca Corp. makes
Medelec, Inc. (Teca Corp.) manufactures disposable and reusable needle electrodes for electromyography (EMG) and nerve conduction studies, including monopolar and myojet designs, as well as electrode systems for nerve conduction testing.
The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. Teca Corp. is headquartered in the United States.
Catalogue
Teca Ncs Electrode System 2000 Ref K971914
Regimes: 510(k) Registry: 510(k)Teca Myoject Disposable Needle Electrodes Ref K973444
Regimes: 510(k) Registry: 510(k)Teca Disposable Monopolar Needle Electrodes Ref K973442
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medelec, Inc. D.B.A. Teca Corp. have in the registry?
The registry currently lists 3 devices for Medelec, Inc. D.B.A. Teca Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medelec, Inc. D.B.A. Teca Corp.'s devices?
Among its 3 most recently registered devices, Medelec, Inc. D.B.A. Teca Corp. has devices listed in FDA 510(k) (3 devices).
What risk classes do Medelec, Inc. D.B.A. Teca Corp.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Medelec, Inc. D.B.A. Teca Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medelec, Inc. D.B.A. Teca Corp. in the registry?
The most recently registered devices listed for Medelec, Inc. D.B.A. Teca Corp. include TECA NCS ELECTRODE SYSTEM 2000, TECA MYOJECT DISPOSABLE NEEDLE ELECTRODES and TECA DISPOSABLE MONOPOLAR NEEDLE ELECTRODES.