Paragonix Technologies, Inc.
Paragonix Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2026, with 1 FDA device recall on record.
Top product codes for Paragonix Technologies, Inc.
FDA recalls by Paragonix Technologies, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Paragonix Technologies, Inc.
- K254305 — BAROguard Donor Lung Preservation System
- K180194 — SherpaPak Cardiac Transport System and SherpaPak Kidney Transport System
- K143054 — Sherpa Pak Kidney Transport System
- K143074 — Sherpa Pak Cardiac Transport System
- K133694 — SHERPA PAK TRANSPORTER
- K133432 — SHERPA PAK CARDIAC TRANSPORT SYSTEM
- K123326 — SHERPA PAK CARDIAC TRANSPORT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.