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 Teftec Corp. with 8 510(k) clearances. The most recent is a 510(k) clearance dated Nov 21, 2002: ALPHATRAC, MODEL A 205.
| Date | Record | Source |
|---|---|---|
| Nov 21, 2002 | ALPHATRAC, MODEL A 205K022652 · ITI | 510(k) clearances |
| Feb 8, 2002 | OMEGATRAC, MODEL Z105K013307 · ITI | 510(k) clearances |
| Nov 18, 1999 | OMEGA TRAC, MODEL Z100K993160 · ITI | 510(k) clearances |
| Oct 25, 1999 | FIRSTCLASS POWER TILT AND RECLINE SEAT SYSTEM, MODEL S400K992628 · ITI | 510(k) clearances |
| Oct 25, 1999 | FIRST CLASS POWER RECLINE SEATING SYSTEM, MODEL S500K992627 · ITI | 510(k) clearances |
| Nov 27, 1998 | FIRSTCLASS POWER TILT SEAT SYSTEM, MODEL S300K983066 · ITI | 510(k) clearances |
| Nov 6, 1998 | ALPHATRAC, MODEL A200K982815 · ITI | 510(k) clearances |
| Jul 1, 1996 | OMEGATRAC BY TEFTECK955240 · ITI | 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
