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 Allo Pro Corp. with 16 510(k) clearances. The most recent is a 510(k) clearance dated Oct 22, 1990: GSB ELBOW.
| Date | Record | Source |
|---|---|---|
| Oct 22, 1990 | GSB ELBOWK901581 · JDC | 510(k) clearances |
| Sep 7, 1990 | SURGICAL COTTON GLOVESK900425 · LYU | 510(k) clearances |
| Mar 1, 1990 | CENTERING PLUGK900392 · LZN | 510(k) clearances |
| Feb 6, 1990 | WEBER PERMALOCKK896669 · LZO | 510(k) clearances |
| Oct 19, 1989 | BIOLOX CERAMIC BALLK892644 · LZO | 510(k) clearances |
| Jan 13, 1989 | RS-CUP ACETABULAR PROSTHESISK885049 · KWA | 510(k) clearances |
| Sep 9, 1987 | KENNEDY STEMK864999 · JDI | 510(k) clearances |
| Jul 13, 1987 | ZWEYMUELLER-SL HIP PROSTHESIS STEMK871453 · KWA | 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
