FirmLabelled 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 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Shenzhen Creative Industry with 11 510(k) clearances and 1 warning letter. The most recent is a 510(k) clearance dated Jan 25, 2021: Pulse Oximeter.
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.
| Jan 25, 2021 | Pulse OximeterK201468 · DQA | 510(k) clearances |
| Dec 31, 2019 | Patient MonitorK192343 · DQA | 510(k) clearances |
| May 8, 2019 | Warning letter: Medical DevicesCDRH | Warning letters |
| Nov 13, 2018 | Handheld Pulse Oximeter, Model SP-20K172792 · DQA | 510(k) clearances |
| Sep 9, 2017 | All-in-One Health Monitor, PC-303K170047 · MWI | 510(k) clearances |
| Jun 3, 2015 | Pulse Oximeter, Models PC-66A; PC-66B; PC-66C;PC-60B1; PC-60B5; PC-60D; PC-60D2; PC-60E; PC-60N; POD-1; POD-2; POD-3; PC-68A; PC-68B; PC-68C; POD- 1W; and POD-60NW-1K150093 · DQA | 510(k) clearances |
| Oct 1, 2013 | PATIENT MONITORK123711 · MWI | 510(k) clearances |
| Dec 7, 2012 | PC-60NW FINGERTIP OXIMETERK120502 · DQA | 510(k) clearances |
| Mar 30, 2010 | VITAL SIGNS MONITORK093016 · DQA | 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
