← FDA DEVICE PRODUCT CODES
FDA PRODUCT CODE · CLASS II
NUH — Stimulator, Nerve, Transcutaneous, Over-The-Counter
TEMPORARY RELIEF OF PAIN DUE TO SORE/ACHING MUSCLES
DEVICE CLASS
Class II
REGULATION
21 CFR 882.5890
MEDICAL SPECIALTY
Neurology
REVIEW PANEL
NE
— Implant— Life-sustaining— GMP-exempt✓ Third-party review eligible
23
510(K)/PMA CLEARANCES
510k: 23
0
RECALL ENTRIES
Recent clearances
K260412Shenzhen Dongdixin Technology Co., Ltd. · 510k2026-06-26
K260425Hivox Biotek, Inc. · 510k2026-06-16
K253896Globalcare Medical Technology Co., Ltd. · 510k2026-03-04
K253305Shenzhen Jiantuo Electronics Co., Ltd. · 510k2025-12-31
K253740Hong Qiangxing (Shenzhen) Electronics Limited · 510k2025-12-23
K251958Dynapulse Medical · 510k2025-12-23
K252688Bozhou Rongjian Medical Appliance Co., Ltd. · 510k2025-11-24
K251856Everyway Medical Instruments Co.,Ltd · 510k2025-11-21
Related on SPEQ
Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.
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