# Tri-Med Specialties, Inc.

- Location (FDA's records): Overland Park, KS
- FDA decisions: 14 (1985–1997): 14 510(k) clearances
- Product codes: LRO (3), KDH (2), KNT (2), OCX (2), KNQ (2), BSS (1), GBT (1), OCZ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 2 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Denver Biomaterials, Inc.: 1 (https://510kreport.com/company/denver-biomaterials)
- Ballard Medical Products: 1 (https://510kreport.com/company/ballard-medical-products)

## Its most-cited devices
- K950574: Needle/Cannula (1995), cited by 1
- K932652: Tri-Med Paracentesis Tray (1993), cited by 1

## Recent decisions
- K971615: Pattison Esophageal Dilator (Jul 24, 1997)
- K970890: #ES-32 Suction Catheter 32 FR. (May 23, 1997)
- K970982: T-RX Retrieval Forceps (May 9, 1997)
- K942918: Tri-Med Endoscopic Fluid Introduction Catheter (Feb 28, 1995)
- K950574: Needle/Cannula (Feb 24, 1995)
- K934348: Tri-Med Quick-Step Gastric Lavage Tube Sizes 18FR, 22FR, 32FR (Dec 23, 1994)
- K945160: Paracentesis Needles/Cannulas (Nov 14, 1994)
- K924549: Tri-Med Quick-Step (TM) Rectal Tube (Feb 10, 1994)

Source page: https://510kreport.com/company/tri-med-specialties