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., part of GE HealthCareLabelled by claude-sonnet-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 14, 2026, FDA's public records list USA Instruments with 64 510(k) clearances. The most recent is a 510(k) clearance dated Nov 9, 2005: USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAY.
| Nov 9, 2005 | USA INSTRUMENTS 3.0T BRAIN/SPINE ARRAYK052916 · MOS | 510(k) clearances |
| Oct 7, 2005 | 1.5T 12 CHANNEL BODY ARRAYK052584 · MOS | 510(k) clearances |
| Oct 7, 2005 | 1.5T 16 CHANNEL BRAIN-SPINE ARRAY COILK052621 · MOS | 510(k) clearances |
| Oct 4, 2005 | 3T HD BREAST ARRAYK052585 · MOS | 510(k) clearances |
| Jun 28, 2005 | OPEN BREAST COIL (OBC) WITH BIOPSY PLATESK050728 · MOS | 510(k) clearances |
| Sep 24, 2004 | MILLENNIUM III 3T-8-CHANNEL NEUROVASCULAR COILK042342 · MOS | 510(k) clearances |
| Aug 26, 2004 | 3.0T 8-CHANNEL CTL SPINE ARRAYK042186 · MOS | 510(k) clearances |
| Aug 26, 2004 | 11000 RAPTURE PHASED ARRAY PERIPHERAL VASCULAR COILK042207 · MOS | 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
