Tenscare, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Tenscare, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Unipro (K-UNIPRO-US), Ova+ (K-OVAP-USA), Unicare (K-UNICARE-USA)
13
Total
13
Cleared
0
Denied
Tenscare, Ltd. has 13 FDA 510(k) cleared medical devices. Based in Timperley, Cheshire, GB.
Latest FDA clearance: Aug 2024. Active since 2001. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Tenscare, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tenscare, Ltd.
13 devices
Cleared
Aug 30, 2024
Unipro (K-UNIPRO-US)
Neurology
382d
Cleared
Dec 15, 2023
Ova+ (K-OVAP-USA)
Neurology
256d
Cleared
Oct 20, 2023
Unicare (K-UNICARE-USA)
Gastroenterology & Urology
197d
Cleared
Aug 18, 2023
Unicare (K-UNICARE-USA)
Neurology
127d
Cleared
Jun 04, 2021
Perfect EMS
Neurology
444d
Cleared
Nov 01, 2019
Perfect PFE
Gastroenterology & Urology
170d
Cleared
Apr 20, 2015
TensCare KegelFit
Gastroenterology & Urology
224d
Cleared
Jun 21, 2011
TENSCARE ITOUCH SURE MODEL ITS
Gastroenterology & Urology
183d
Cleared
Feb 09, 2009
TENSCARE ITOUCH MODEL(S) EASY AND PLUS
Neurology
175d
Cleared
Mar 03, 2003
TENSCARE ULTIMA NMS/EMS
Physical Medicine
90d
Cleared
May 21, 2002
ULTIMA TENS XL-A1
Neurology
67d
Cleared
Aug 31, 2001
TENS CARE, MODEL XL-Y3
Neurology
105d