Shenzhen RF Tech Co., Ltd.

FDA Regulatory Profile

Shenzhen RF Tech Co., Ltd. appears in FDA public data with 0 recalls, 12 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 14, 2026.

Summary

Total Recalls
0
510(k) Clearances
12
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252587HD 8Ch Wrist ArrayApril 14, 2026
K252876GEM Flex Coil 16-L Array, 3.0T Receive Only; GEM Flex Coil 16-M Array, 3.0T Receive Only; GEM Flex CApril 1, 2026
K252179GEM Flex Coil 16-L Array, 1.5T Receive Only; GEM Flex Coil 16-M Array, 1.5T Receive Only; GEM Flex CFebruary 10, 2026
K2310851.5T HD T/R Knee Array (10-F34127)August 18, 2023
K2232031.5T 24E Posterior ArrayMarch 2, 2023
K2232258ch T/R Knee CoilFebruary 14, 2023
K2232398ch Wrist CoilDecember 8, 2022
K2008368ch Flex SuiteJuly 22, 2020
K1722228ch Flex SuiteDecember 8, 2017
K1609328ch Foot Ankle CoilAugust 1, 2016
K1609358ch Foot Ankle CoilJuly 28, 2016
K1516538ch Foot Ankle CoilAugust 7, 2015