Tenscare, Ltd. is one of 428 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.
510(k) submissions have been managed by Akos (Meddiquest) as regulatory consultant.
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