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 14, 2026, FDA's public records list Medical Engineering Corp. with 28 510(k) clearances. The most recent is a 510(k) clearance dated Nov 18, 1993: STAND ALONE CYSTOMETROGRAM.
| Nov 18, 1993 | STAND ALONE CYSTOMETROGRAMK934141 · FEN | 510(k) clearances |
| Mar 13, 1991 | SURGITEK(R) LUBRI-FLEX(TM) URETERAL STENTK905289 · FAD | 510(k) clearances |
| Jan 14, 1991 | SURGITEK TEX-SPAN TEXTURED TISSUE EXPANDERK903448 · LCJ | 510(k) clearances |
| Jul 16, 1990 | SURGITEK(R) FLEXIBLE URETEROSCOPY INTRO/SHEATH SETK902773 · FGB | 510(k) clearances |
| Aug 10, 1989 | SURGITEK FLAT T-SPANK884746 · LCJ | 510(k) clearances |
| Feb 8, 1989 | SURGITEK (R) UROFLOW SYSTEMK883274 · FFG | 510(k) clearances |
| Aug 11, 1988 | SURGITEK CO2 DELIVERY SYSTEMK881736 · FAP | 510(k) clearances |
| May 26, 1988 | SURGITEK FLEXIBLE URETEROSCOPE SU-7 & SU-9K880801 · FGB | 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
