Tyrx, Inc.
Tyrx, Inc. holds FDA 510(k) medical device clearances, first cleared 2010, most recent 2015, with 3 FDA device recalls on record.
Top product codes for Tyrx, Inc.
FDA recalls by Tyrx, Inc.
- Z-2541-2016 — TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
- Z-2539-2016 — TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
- Z-2540-2016 — TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for stabilization of implanted pacemakers (IPG) and/or implantable cardioverter defibrillators (ICD)
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 Tyrx, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.