Dantec Electronics, Inc.
United StatesFDA applicant, unverified
- Devices
- 12
What Dantec Electronics, Inc. makes
Dantec Electronics, Inc. manufactures disposable and reusable electrodes for nerve and muscle stimulation, including pudendal, sphincter, and sensory needle electrodes. Their portfolio also includes urodynamic devices such as catheter tip transducers, uroflowmeters, and stimulators for bladder and pelvic floor assessment. Additional products include concentric electrodes for nerve conduction studies and systems for automated electrodiagnostic testing.
The company’s devices are classified under FDA’s Class I and Class II categories, with regulatory submissions recorded in the FDA’s 510(k) clearance registry. These products are intended for diagnostic and therapeutic applications in urology, neurology, and electrophysiology. The manufacturer is based in the United States.
Catalogue
Search and filter all 12 devicesFrequently asked questions
How many devices does Dantec Electronics, Inc. have in the registry?
The registry currently lists 12 devices for Dantec Electronics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dantec Electronics, Inc.'s devices?
Among its 12 most recently registered devices, Dantec Electronics, Inc. has devices listed in FDA 510(k) (12 devices).
What risk classes do Dantec Electronics, Inc.'s devices fall under?
Among its 12 most recently registered devices, the classes recorded for Dantec Electronics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dantec Electronics, Inc. in the registry?
The most recently registered devices listed for Dantec Electronics, Inc. include DANTEC 13L40 ST. MARKS'S PUDENDAL ELECTRODE, DANTEC COUNTERPOINT, SENSORY NEEDLE ELECTRODE DNE 111-115, 116-117, 118 and DANTEC MAGNETIC STIMULATOR.