# Martech Medical Products, Inc.

- Location (FDA's records): Harleysville, PA
- FDA decisions: 11 (1989–2026): 11 510(k) clearances
- Names in FDA's records: Martech Medical Products, Inc. (7); Martech Medical Products (4)
- Product codes: DYB (3), JKA (2), CCL (1), FBK (1), FMF (1), FMI (1), CBT (1), PTI (1)
- Predicates its devices cite: 9 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Medcomp: 4 (https://510kreport.com/company/medcomp)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Mill-Rose Laboratory: 1 (https://510kreport.com/company/mill-rose-laboratory)
- Xentek Medical, Inc.: 1 (https://510kreport.com/company/xentek-medical)
- Jiangsu Caina Medical Co.,Ltd: 1 (https://510kreport.com/company/jiangsu-caina-medical)

## Firms that cite its devices most
- Medcomp ( Medical Components): 1 (https://510kreport.com/company/medcomp-medical-components)
- Cook Urological, Inc.: 1 (https://510kreport.com/company/cook-urological)
- Advanced Uroscience, Inc.: 1 (https://510kreport.com/company/advanced-uroscience)

## Its most-cited devices
- K960519: Martech Endoscopic Injection Needle (1996), cited by 2
- K120617: Ptfe Super Sheath Introducer (2012), cited by 1
- K130855: Ptfe Super Sheath Introducer (2013), cited by 1

## Recent decisions
- K254095: 25G Huber Needle (Sep 18, 2026)
- K130855: Ptfe Super Sheath Introducer (Jul 29, 2013)
- K120617: Ptfe Super Sheath Introducer (Nov 19, 2012)
- K101399: Coaxial Introducer Set (Jun 17, 2010)
- K960519: Martech Endoscopic Injection Needle (May 1, 1996)
- K931924: Marksman Arterial Blood Gas Syringe (Aug 3, 1993)
- K922438: PRO2 Oxygen Analyzer (Mar 5, 1993)
- K926007: Accessory to Piston Syringe (Feb 23, 1993)

Source page: https://510kreport.com/company/martech-medical-products