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 15, 2026, FDA's public records list Sunmax Enterprise Shanghai Co., Ltd. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 1, 2009: SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED….
| Jul 1, 2009 | SUNMAX ENTERPRISE SHANGHAI CO. POWDER FREE BLUE NITRILE PATIENT EXAMINATION GLOVE TESTED WITH CHEMOTHERAPY DRUGSK090336 · LZA | 510(k) clearances |
| Aug 16, 2001 | SUNMAX BLUE NITRILE POWDER-FREE EXAMINATION GLOVEK011765 · LZA | 510(k) clearances |
| Aug 14, 2001 | SUNMAX BLUE NITRILE POWDERED EXAMINATION GLOVESK011717 · LZA | 510(k) clearances |
| Feb 7, 1997 | POWDER-FREE VINYL PATIENT EXAMINATION GLOVESK964964 · LYZ | 510(k) clearances |
| Jun 27, 1996 | SUNMAX ENTERPRISE SHANGHAI VINYL POWDERED PATIENT EXAM. GLOVESK960746 · LYZ | 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
