Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Marina Medical Instruments with 5 510(k) clearances. The most recent is a 510(k) clearance dated May 10, 2005: MARINA MEDICAL FINGER PROTECTORS.
| May 10, 2005 | MARINA MEDICAL FINGER PROTECTORSK042534 · KGO | 510(k) clearances |
| Nov 18, 2003 | MARINA MEDICAL SILICONE PESSARYK031463 · HHW | 510(k) clearances |
| Apr 8, 2003 | MAS WITH OR WITHOUT SYRINGEK021876 · HHK | 510(k) clearances |
| Feb 3, 2003 | HEMORRHAGE OCCLUDER PIN (HOP), MODEL 337-247K023725 · GDW | 510(k) clearances |
| Apr 11, 2001 | UTERINE MANIPULATOR INJECTOR CANNULA, MODEL R57-450K010296 · LKF | 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
