Home › EVERYWAY MEDICAL INSTRUMENTS CO., LTD. › Everyway
Everyway
EVERYWAY MEDICAL INSTRUMENTS CO., LTD. · Model EV-804P · UDI-DI 04719871183540
10
510(k) clearances
118
Adverse events
0
Recalls
169
Facilities
Description
Transcutaneous Electrical Nerve Stimulator (T.E.N.S.)
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.