Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in ChinaLabelled 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 Shenzhen RF Tech with 12 510(k) clearances. The most recent is a 510(k) clearance dated Apr 14, 2026: HD 8Ch Wrist Array.
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.
| Apr 14, 2026 | HD 8Ch Wrist ArrayK252587 · MOS | 510(k) clearances |
| Apr 1, 2026 | GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex Coil 16-S Array, 3.0T Receive OnlyK252876 · MOS | 510(k) clearances |
| Feb 10, 2026 | GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex Coil 16-S Array, 1.5T Receive OnlyK252179 · MOS | 510(k) clearances |
| Aug 18, 2023 | 1.5T HD T/R Knee Array (10-F34127)K231085 · MOS | 510(k) clearances |
| Mar 2, 2023 | 1.5T 24E Posterior ArrayK223203 · LNH | 510(k) clearances |
| Feb 14, 2023 | 8ch T/R Knee CoilK223225 · MOS | 510(k) clearances |
| Dec 8, 2022 | 8ch Wrist CoilK223239 · MOS | 510(k) clearances |
| Jul 22, 2020 | 8ch Flex SuiteK200836 · MOS | 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
