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.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Surgical Appliance Industries, Inc. with 9 510(k) clearances. The most recent is a 510(k) clearance dated Apr 27, 2012: TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR COMPRESSION GAUNTLET.
| Apr 27, 2012 | TRUFORM READY-TO-WEAR COMPRESSION ARM SLEECE TRUFORM READY-TO-WEAR COMPRESSION GAUNTLETK121106 · DWL | 510(k) clearances |
| Jun 24, 1982 | TRUNCAL ORTHOSISK821682 · IQE | 510(k) clearances |
| Jan 18, 1982 | EXTERNAL BREAST PROSTHESISK813416 · GBI | 510(k) clearances |
| Sep 14, 1981 | NEOPRENE KNEE SUPPORTK812423 · ITQ | 510(k) clearances |
| Sep 14, 1981 | CRUCIFORM ANTERIOR SPINAL HYPEREXTEN. OK812401 · IPT | 510(k) clearances |
| Sep 14, 1981 | CUSTOM CONTOUR LUMBOSACRAL ORTHOSISK812422 · IPY | 510(k) clearances |
| Jun 25, 1981 | ANKLE-FOOT CAST/SPLINTK811690 · IQI | 510(k) clearances |
| Jun 25, 1981 | CYLINDER KNEE CAST/SPLINTK811689 · ITQ | 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
