Scientia Vascular, Inc.
Scientia Vascular, Inc. holds FDA 510(k) medical device clearances, first cleared 2023, most recent 2026, with 3 FDA device recalls on record.
Top product codes for Scientia Vascular, Inc.
FDA recalls by Scientia Vascular, Inc.
- Z-1235-2025 — Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices and embolization materials and infusion of diagnostic agents to the neuro and peripheral vasculature during interventional or diagnostic procedures.
- Z-1234-2025 — Socrates 38 Aspiration Catheter 127 cm length REF SC038-127-001 The Socrates Aspiration System with a compatible suction pump is intended for use in the revascularization of patients with acute ischemic stroke
- Z-1249-2023 — Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
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 Scientia Vascular, Inc.
- K260223 — Aristotle Mini Guidewire
- K260002 — Socrates Aspiration System (Socrates 70 Aspiration Catheter)
- K253579 — Aristotle 14 Guidewire; Aristotle 18 Guidewire; Aristotle 24 Guidewire; Zoom Wire 14 Guidewire
- K243938 — Aristotle 14 Guidewire +4 more
- K242301 — Socrates 38 Catheter
- K223913 — Socrates Aspiration System
- K223560 — Plato 17 Microcatheter
- K231954 — Aristotle 18 Guidewire; Aristotle 24 Guidewire
- K222437 — Aristotle Colossus Guidewire
Data sourced from openFDA. This site is unofficial and independent of the FDA.