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Dilator, Vessel, Surgical
FDA product code DWP · Class 2 · Cardiovascular
1,238
Registered devices
171
Adverse events
1
Recalls
20
510(k) clearances
Devices with this code
V. Mueller — STERIS CORPORATIONGarrett Vessel Probe 14cm 3.0mm — Geister Medizintechnik GmbHGARRETT VASCULAR DILATOR — SONTEC INSTRUMENTS, INC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPILLING — TELEFLEX INCORPORATEDDilator, Vascular, acc. Geister 15cm 3.0mm alu-handle PURPLE — Geister Medizintechnik GmbHAvalign — Avalign Technologies, Inc.Mitchell Aortic Valve Dilator — SONTEC INSTRUMENTS, INC.Dilator, Vascular, Memory 20cm 6.0mm alu-handle — Geister Medizintechnik GmbHNovo Surgical — NOVO SURGICAL, INC.Ambler Surgical — AMBLER SURGICAL CORP.SCANLAN® Dilator — SCANLAN INTERNATIONAL INCVascular Probe Extra Supple — SYNOVIS LIFE TECHNOLOGIES, INC.Mitchell Aortic Valve Dilator — SONTEC INSTRUMENTS, INC.Symmetry Surgical® — ASPEN SURGICAL PRODUCTS, INC.Symmetry OPTI-LENGTH® GARRETT — ASPEN SURGICAL PRODUCTS, INC.Millennium — Avalign Technologies, Inc.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.BARD® PARSONNET — Bard Peripheral Vascular, Inc.Ambler Surgical — AMBLER SURGICAL CORP.AESCULAP — AESCULAP, INC.Dilator, Vascular, acc. Garrett 14cm 2.25mm — Geister Medizintechnik GmbHMITCHELL AORTIC VALVE DILATOR — SONTEC INSTRUMENTS, INC.Dilator, Vascular, Memory 14cm 3.0mm monobloc — Geister Medizintechnik GmbH
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2023-12-06 | Baxter Healthcare Corporation | Cardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align wi |
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