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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K223438

TELIGEN System Peripheral Motor Nerve Stimulation Indications · Medos International SARL · decided 2023-02-10 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
TELIGEN286202205SMedos International SàrlOLO PDQ10705034604558
SENTIO186002110SMedos International SàrlPDQ10705034560366
TELIGEN186000000SMedos International SàrlGAD HRX LXH OLO PDQ10705034560359
TELIGEN286006062SMedos International SàrlOLO PDQ10705034604527