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 Trebay Medical Corp. with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jan 30, 1996: TREBAY MICRODEBRIDER SYSTEM.
| Jan 30, 1996 | TREBAY MICRODEBRIDER SYSTEMK955704 · EQJ | 510(k) clearances |
| Dec 22, 1995 | TREBAY SCOPE IRRIGATED CLEARING SLEEVEK955560 · EOB | 510(k) clearances |
| Dec 22, 1995 | SOF - ABRASION BURK955294 · EQJ | 510(k) clearances |
| Dec 21, 1995 | TYMPANOSTOMY TUBEK955447 · ETD | 510(k) clearances |
| Dec 6, 1995 | TREBAY IRRIGATED CUTTER BLADE (MODIFICATION)K954912 · EQJ | 510(k) clearances |
| Nov 15, 1995 | AT2 & DOYLE STYLE (C-FLEX) VENT TUBESK954795 · ETD | 510(k) clearances |
| Nov 6, 1995 | MICRO-INGRESSOR HANDIPIECEK954796 · ERL | 510(k) clearances |
| Oct 27, 1995 | MICRO-PLANER HANDPIECEK954715 · ERL | 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
