INTELLICARE CO., LTD.

FDA registration

INTELLICARE CO., LTD.·1 product·🇭🇰 Hong Kong

Hammacher Schlemmer (KTR-2493)

FDA registration

SHENZHEN KENTRO MEDICAL ELECTRONICS CO., LTD·1 product·🇨🇳 China

PP904

FDA registration

HIVOX Electronics Co., Ltd.·1 product·🇨🇳 China

LOW BACK PAIN RELIEF SYSTEM

FDA registration

GEMORE TECHNOLOGY CO., LTD.·1 product·🇹🇼 Taiwan

TENS

FDA registration

JKH Health Co., Ltd.·1 product·🇨🇳 China

Samsung ECG Monitor App with Irregular Heart Rhythm Notification

FDA UDI

Samsung Electronics Co., Ltd.·08806094948240·The Samsung ECG Monitor Application with Irregu...

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005258·ActiPatch Muscle and Joint Pain Therapy Kit 5 pack

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005241·ActiPatch Knee Pain Therapy Device 5 pack

ActiPatch

FDA UDI

Bioelectronics Corporation·80851329005155·ActiPatch Back Pain Therapy Kit 5 pack

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005159·Back Pain Advanced Long-Lasting Relief

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005203·Back , Knee, Muscle and Joint 7 day trial

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005340·Back, Knee, Muscle & Joint Advanced Long-Lastin...

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005470·ActiPatch Back Pain Relief Therapy 100 pack

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005494·ActiPatch Muscle and Joint Relief Therapy 100 pack

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005012·Knee Pain Advanced Long-Lasting Relief

ActiPatch

FDA UDI

Bioelectronics Corporation·00851329005487·ActiPatch Knee Pain Relief Therapy 100 pack

Samsung ECG Monitor App with Irregular Heart Rhythm Notification

FDA UDI

Samsung Electronics Co., Ltd.·08806094948233·The Samsung ECG Monitor Application with Irregu...

KT RECOVERY+ WAVE

FDA UDI

Bioelectronics Corporation·00851329005463·KT RECOVERY+ WAVE Electromagnetic Pain Relief

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·NEEDLE-EASE TM 2501

Sharps Needle Destruction Device

FDA Pre-Market Approval

FDA Class 2 ·NEEDLE-EASE MODEL 3500