Tenscare, Ltd.
Tenscare, Ltd. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2024.
Top product codes for Tenscare, Ltd.
Recent clearances by Tenscare, Ltd.
- K232441 — Unipro (K-UNIPRO-US)
- K230926 — Ova+ (K-OVAP-USA)
- K230983 — Unicare (K-UNICARE-USA)
- K231053 — Unicare (K-UNICARE-USA)
- K200694 — Perfect EMS
- K191312 — Perfect PFE
- K142506 — TensCare KegelFit
- K103698 — TENSCARE ITOUCH SURE MODEL ITS
- K082377 — TENSCARE ITOUCH MODEL(S) EASY AND PLUS
- K023997 — TENSCARE ULTIMA NMS/EMS
- K020846 — ULTIMA TENS XL-A1
- K011543 — TENS CARE, MODEL XL-Y3
- K003591 — TENSCARE, MODEL TENS XL-2
Data sourced from openFDA. This site is unofficial and independent of the FDA.