Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United KingdomLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Tenscare Ltd. with 13 510(k) clearances. The most recent is a 510(k) clearance dated Aug 30, 2024: Unipro (K-UNIPRO-US).
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Aug 30, 2024 | Unipro (K-UNIPRO-US)K232441 · GZJ | 510(k) clearances |
| Dec 15, 2023 | Ova+ (K-OVAP-USA)K230926 · NUH | 510(k) clearances |
| Oct 20, 2023 | Unicare (K-UNICARE-USA)K230983 · KPI | 510(k) clearances |
| Aug 18, 2023 | Unicare (K-UNICARE-USA)K231053 · NUH | 510(k) clearances |
| Jun 4, 2021 | Perfect EMSK200694 · NUH | 510(k) clearances |
| Nov 1, 2019 | Perfect PFEK191312 · KPI | 510(k) clearances |
| Apr 20, 2015 | TensCare KegelFitK142506 · KPI | 510(k) clearances |
| Jun 21, 2011 | TENSCARE ITOUCH SURE MODEL ITSK103698 · KPI | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
