# Pioneering Technologies, Inc.

- Location (FDA's records): Wheat Ridge, CO
- FDA decisions: 19 (1988–1992): 19 510(k) clearances
- Product codes: DWS (3), DSY (3), DWF (2), DXC (2), KRH (1), DWP (1), DRE (1), KGO (1), EFQ (1), GXY (1), DWC (1), GAQ (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 6 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Genesee Biomedical, Inc.: 4 (https://510kreport.com/company/genesee-biomedical)
- Uni-Patch, Inc.: 1 (https://510kreport.com/company/uni-patch)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Its most-cited devices
- K905175: Pti Annuloplasty Ring (Sterile) (1992), cited by 5
- K901575: Reusable Tens Paravertebral Pad #641 Back Electrod (1990), cited by 1

## Recent decisions
- K922025: Anastomart (TM) Coronary Bypass Graft Markers/Modif (Sep 22, 1992)
- K905175: Pti Annuloplasty Ring (Sterile) (Feb 14, 1992)
- K905068: Pti Intra-Art (TM) Pick-UP Wicks (Dec 31, 1991)
- K910067: Pti Sternal Closure Wire Suture (May 6, 1991)
- K905067: Pti Anastomark Flexible Coronary Bypass Graft (Mar 18, 1991)
- K901815: Modified Sterilization of Intra-Art (TM) Coronary (Jul 3, 1990)
- K901682: Pti Anastomark (TM) Coronary Bypass Graft Markers (Jul 3, 1990)
- K901531: Pti Intra-Artr Reusable Coronary Artery Probe (Jun 20, 1990)

Source page: https://510kreport.com/company/pioneering-technologies