FirmLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list United Pacific Co., Ltd. with 6 510(k) clearances and 1 drug recall. The most recent is a drug recall dated Mar 29, 2018: Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 10….
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.
| Mar 29, 2018 | Zhong Hua Jiu (menthol 1%) Patch, Distributed by United Pacific Company, UPC 6 924938 100226, NDC 53614-001-02Class II · CGMP Deviations: the product was produced with substandard GMP manufacturing processes. | Drug recalls |
| Sep 12, 2003 | THERMOSKIN CONDUCTIVE PADSK030564 · GXY | 510(k) clearances |
| Oct 19, 2000 | SPIRIT ACUPUNCTURE NEEDLEK003010 · MQX | 510(k) clearances |
| Jun 21, 2000 | MILLENNIA ACUPUNCTURE NEEDLEK001718 · MQX | 510(k) clearances |
| Dec 17, 1999 | QK-WIDE BAND SPECTRUM THERAPEUTIC APPARATUS, MODELS CO1A, CO1B, CO1C, CO1D, CO2A, CO2BK993123 · ILY | 510(k) clearances |
| Jul 28, 1999 | SACRED CRANE TDP LAMP, MODELS CQ-27, CQ-12, CQ-36K991503 · ILY | 510(k) clearances |
| Apr 16, 1999 | KINGLI ACUPUNCTURE NEEDLEK990406 · MQX | 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
