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 American Midwest with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jul 16, 1982: AH-1 LIGHT-CURE DENTAL COMPOSITE RESTOR.
| Jul 16, 1982 | AH-1 LIGHT-CURE DENTAL COMPOSITE RESTORK821895 · EBF | 510(k) clearances |
| Jun 25, 1982 | AM-40 SYSTEMK821715 · EFB | 510(k) clearances |
| Apr 9, 1982 | MIDWEST LIGHT WANDK820693 · EBZ | 510(k) clearances |
| Aug 18, 1981 | ATT-1 DENTAL COMPOSITE RESTORATIVE SYSK811979 · EBF | 510(k) clearances |
| Apr 10, 1980 | U-STYLE ADAPTERK800735 · EGS | 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
