Medical device makerLabelled 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 Globe Ent., Inc. with 5 510(k) clearances. The most recent is a 510(k) clearance dated Dec 17, 1997: PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S PRELIMINARY.
| Date | Record | Source |
|---|---|---|
| Dec 17, 1997 | PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S PRELIMINARYK972854 · FPA | 510(k) clearances |
| Dec 17, 1997 | PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SETK972839 · FPA | 510(k) clearances |
| Dec 16, 1997 | PROTOS BLOOD TRANSFUSION SETK972843 · BRZ | 510(k) clearances |
| Sep 11, 1989 | PATIENT EXAMINATION GLOVES (LATEX)K892623 · LYY | 510(k) clearances |
| Mar 14, 1989 | SURGICAL GLOVESK884622 · KGO | 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
