Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Transcorp, Inc. with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jul 5, 2013: TRANSCORP ACIF SYSTEM.
| Jul 5, 2013 | TRANSCORP ACIF SYSTEMK121178 · ODP | 510(k) clearances |
| Apr 16, 2012 | TRANSCORP SPINAL ACCESS SYSTEMK113352 · HRX | 510(k) clearances |
| Sep 13, 2010 | TRANSCORP ACIF SYSTEMK092794 · ODP | 510(k) clearances |
| May 21, 2010 | TRANSCORP TRANS-PLATE ANTERIOR CERVICAL PLATE SYSTEMK092695 · KWQ | 510(k) clearances |
| May 13, 1993 | LATEX EXAMINATION GLOVESK922439 · LYY | 510(k) clearances |
| Feb 27, 1992 | STERILETX POWDER FREE LATEX EXAMINATION GLOVESK915189 · LYY | 510(k) clearances |
| Jan 11, 1991 | SRI JOHANI LATEX SURGEONS GLOVESK904662 · KGO | 510(k) clearances |
| Aug 7, 1990 | KLEARTEX LATEX SURGICAL GLOVESK903069 · KGO | 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
