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 Del Global TechnologiesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Del Medical with 4 510(k) clearances and 2 device recalls. The most recent is a 510(k) clearance dated Apr 10, 2023: DMX.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Apr 10, 2023 | DMXK223550 · KPR | 510(k) clearances |
| Nov 20, 2017 | MDR17 Mobile Direct Radiographic SystemK173018 · IZL | 510(k) clearances |
| Dec 14, 2015 | OTC12D AUTO RADIOGRAPHIC SYSTEMK152767 · KPR | 510(k) clearances |
| Dec 3, 2015 | VS200 radiographic Cassette Holder or Wall Stand. For use in radiology department.Class II · The wall stand cassette holder can suddenly fall to the bottom of its travel, near the ground and contact patient. | Device recalls |
| Dec 3, 2015 | VS300 radiographic Cassette Holder or Wall Stand. For use in radiology department.Class II · The wall stand cassette holder can suddenly fall to the bottom of its travel, near the ground and contact patient. | Device recalls |
| Jul 17, 2014 | DELWORKS DR SYSTEMK140825 · MQB | 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
