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 13, 2026, FDA's public records list Acra Cut, Inc. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 8, 2003: ACRA-CUT XPRESS 120.
| Dec 8, 2003 | ACRA-CUT XPRESS 120K032970 · HBF | 510(k) clearances |
| Nov 18, 1994 | ACRA-CUTK944311 · HBO | 510(k) clearances |
| Sep 10, 1991 | ACRA-CUT WIRE PASS DRILLK911812 · HBE | 510(k) clearances |
| Sep 10, 1991 | ACRA-CUT NEUROLOGICAL SURGICAL DEVICE-POWEREDK911819 · HBE | 510(k) clearances |
| Feb 12, 1991 | DURAL DISSECTORSK910226 · HAO | 510(k) clearances |
| Feb 12, 1991 | BONE PAD REMOVERK910225 · HAO | 510(k) clearances |
| Jun 15, 1989 | AUTOMATIC CRANIAL DRILL (PERFORATOR)K892866 · HBF | 510(k) clearances |
| Dec 29, 1983 | ACRA-CUTK833266 · HBF | 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
