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 Medicor USA, Ltd. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jul 18, 1986: MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEM.
| Jul 18, 1986 | MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEMK861994 · KPR | 510(k) clearances |
| Jun 19, 1986 | MODEL RS-3 RADIOGRAPHIC STANDK861995 · IYB | 510(k) clearances |
| May 7, 1986 | MODEL MS-325 RADIOGRAPHIC X-RAY GENERATORK860025 · KPR | 510(k) clearances |
| Sep 19, 1985 | MODEL PCX/EMY 525A MICROPROCESSSOR CONTROL X-RAY CK850761 · BZN | 510(k) clearances |
| Jul 1, 1985 | MODEL BION 2/TYPE 90 ROOM IONIZERK851358 · FRF | 510(k) clearances |
| Jun 19, 1985 | MODEL BION 1/TYPE 1084T CAR IONIZERK851094 · FRF | 510(k) clearances |
| Nov 27, 1984 | FLOOR MOUNTED X-RAY TUBESTANDK843335 · IYB | 510(k) clearances |
| Mar 23, 1984 | UROLIX-3 UROLOGICAL TABLEK840227 · IXR | 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
