Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled 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 Tri-Med Specialties with 14 510(k) clearances. The most recent is a 510(k) clearance dated Jul 24, 1997: PATTISON ESOPHAGEAL DILATOR.
| Jul 24, 1997 | PATTISON ESOPHAGEAL DILATORK971615 · KNQ | 510(k) clearances |
| May 23, 1997 | #ES-32 SUCTION CATHETER 32 FR.K970890 · KNT | 510(k) clearances |
| May 9, 1997 | T-RX RETRIEVAL FORCEPSK970982 · OCZ | 510(k) clearances |
| Feb 28, 1995 | TRI-MED ENDOSCOPIC FLUID INTRODUCTION CATHETERK942918 · OCX | 510(k) clearances |
| Feb 24, 1995 | NEEDLE/CANNULAK950574 · LRO | 510(k) clearances |
| Dec 23, 1994 | TRI-MED QUICK-STEP GASTRIC LAVAGE TUBE SIZES 18FR, 22FR, 32FRK934348 · BSS | 510(k) clearances |
| Nov 14, 1994 | PARACENTESIS NEEDLES/CANNULASK945160 · LRO | 510(k) clearances |
| Feb 10, 1994 | TRI-MED QUICK-STEP(TM) RECTAL TUBEK924549 · GBT | 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
