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 13, 2026, FDA's public records list Sonoscape Company Limited with 22 510(k) clearances. The most recent is a 510(k) clearance dated Apr 28, 2015: S30/S40 Digital Color Doppler Ultraound System.
| Date | Record | Source |
|---|---|---|
| Apr 28, 2015 | S30/S40 Digital Color Doppler Ultraound SystemK150045 · IYN | 510(k) clearances |
| Jan 29, 2015 | S8 Exp/S9 Pro Portable Digital Color Doppler Ultrasound SystemK142714 · IYN | 510(k) clearances |
| Jan 28, 2015 | S22 Digital Color Doppler Ultrasound SystemK142815 · IYN | 510(k) clearances |
| Jan 5, 2015 | S9 Portable Digital Color Doppler Ultrasound SystemK142710 · IYN | 510(k) clearances |
| Dec 19, 2014 | S12 Digital Color Doppler Ultrasound SystemK142474 · IYN | 510(k) clearances |
| Nov 14, 2013 | DIGITAL COLOR DOPPLER ULTASOUND SYSTEMK132527 · IYN | 510(k) clearances |
| Nov 14, 2013 | DIGITAL ELECTROCARDIOGRAPHSK131262 · DPS | 510(k) clearances |
| Oct 4, 2013 | S8 EXP PORTABLE DIGITAL COLOR DOPPLER ULTRASOUND SYSTEMK132768 · IYN | 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
