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 Terray Manufacturing with 9 510(k) clearances. The most recent is a 510(k) clearance dated Feb 3, 1992: THORACIC ANTERIOR SPINAL FIXATION PLATE.
| Feb 3, 1992 | THORACIC ANTERIOR SPINAL FIXATION PLATEK910874 · KWQ | 510(k) clearances |
| Oct 13, 1988 | CASF CANCELLOUS BONE SCREW, BT650K882934 · HWC | 510(k) clearances |
| Sep 23, 1988 | CASF DRILL GUIDE DG 170K882871 · LYQ | 510(k) clearances |
| Aug 10, 1988 | CASF STERILIZATION TRAYK883125 · FSM | 510(k) clearances |
| Aug 10, 1988 | CASF STERILIZATION TRAYK883193 · FSM | 510(k) clearances |
| Jun 30, 1987 | ANTERIOR SPINAL FIXATION PLATEK870085 · KWP | 510(k) clearances |
| May 6, 1987 | BONE PLATEK870082 · HRS | 510(k) clearances |
| Feb 26, 1987 | FERRAY EXTRACTORK870083 · HWB | 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
