ClearanceBrief
Company ยท GB

Tenscare, Ltd.

FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2024. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GZJStimulator, Nerve, Transcutaneous, For Pain Relief5
KPIStimulator, Electrical, Non-Implantable, For Incontinence4
NUHStimulator, Nerve, Transcutaneous, Over-The-Counter3
IPFStimulator, Muscle, Powered1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Aug 30, 2024K232441Unipro (K-UNIPRO-US)
Tenscare, Ltd., GB
GZJ
Dec 15, 2023K230926Ova+ (K-OVAP-USA)
Tenscare, Ltd., GB
NUH
Oct 20, 2023K230983Unicare (K-UNICARE-USA)
Tenscare, Ltd., GB
KPI
Aug 18, 2023K231053Unicare (K-UNICARE-USA)
Tenscare, Ltd., GB
NUH
Jun 4, 2021K200694Perfect EMS
Tenscare, Ltd., GB
NUH
Nov 1, 2019K191312Perfect PFE
Tenscare, Ltd., GB
KPI
Apr 20, 2015K142506TensCare KegelFit
Tenscare, Ltd., GB
KPI
Jun 21, 2011K103698TENSCARE ITOUCH SURE MODEL ITS
Tenscare, Ltd., GB
KPI
Feb 9, 2009K082377TENSCARE ITOUCH MODEL(S) EASY AND PLUS
Tenscare, Ltd., GB
GZJ
Mar 3, 2003K023997TENSCARE ULTIMA NMS/EMS
Tenscare, Ltd., GB
IPF
May 21, 2002K020846ULTIMA TENS XL-A1
Tenscare, Ltd., GB
GZJ
Aug 31, 2001K011543TENS CARE, MODEL XL-Y3
Tenscare, Ltd., GB
GZJ
Feb 14, 2001K003591TENSCARE, MODEL TENS XL-2
Tenscare, Ltd., GB
GZJ

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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