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 15, 2026, FDA's public records list U.S. Medical Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Jul 5, 1994: U. S. MEDICAL PS-3500 WARMER/INCUBATOR SCALE.
| Jul 5, 1994 | U. S. MEDICAL PS-3500 WARMER/INCUBATOR SCALEK934677 · FMT | 510(k) clearances |
| May 26, 1993 | U.S. MEDICAL PS-7000 DIALYSIS SCALEK924440 · KOE | 510(k) clearances |
| Feb 12, 1993 | U.S. MEDICAL PS-6000 WHEELCHAIR SCALEK924441 · INF | 510(k) clearances |
| Mar 21, 1991 | U.S. MEDICAL PS-1000 PEDIATRIC SCALEK910581 · FRW | 510(k) clearances |
| Mar 21, 1991 | U.S. MEDICAL PS-2000 PEDIATRIC SCALEK910582 · FRW | 510(k) clearances |
| Mar 21, 1991 | U.S. MEDICAL PS-3000 NEONATAL SCALEK910583 · FRW | 510(k) clearances |
| Feb 1, 1990 | AUTO-CUFF(TM)K896633 · DXN | 510(k) clearances |
| Jun 4, 1980 | PULSED GALVANIC STIMULATOR, 450-DYNAMAXK801053 · IPF | 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
