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Transcutaneous Electrical Nerve Stimulators

Shenzhen Kentro Medical Electronics Co.,Ltd · Model KTR-2210 · UDI-DI 06924607702249

NUHNGX
1
510(k) clearances
118
Adverse events
0
Recalls
169
Facilities

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Data 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.