Cordis Corporation
Cordis Corporation holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2022, with 39 FDA device recalls on record.
Top product codes for Cordis Corporation
FDA recalls by Cordis Corporation
10 most recent of 39- Z-0220-2022 — SMART FLEX 10x100 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
- Z-0221-2022 — SMART FLEX 10x100 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
- Z-0218-2022 — SMART FLEX 6x150 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
- Z-0216-2022 — SMART FLEX 9x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
- Z-0217-2022 — SMART FLEX 6x120 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
- Z-0219-2022 — SMART FLEX 8x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
- Z-2431-2021 — Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
- Z-2432-2021 — Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598C
- Z-2430-2021 — Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598A
- Z-2428-2021 — Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
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 Cordis Corporation
- K220654 — ANGIOGUARD XP Emboli Capture Guidewire, ANGIOGUARD RX Emboli Capture Guidewire
- K212977 — SUPER TORQUE MB Angiographic Catheter with Radiopaque markerbands
- K210626 — SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
- K202167 — Brite Tip Radianz Guiding Sheath
- K201377 — SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter
- K201333 — SABER .035 PTA Dilatation Catheter
- K181592 — RAIN Sheath Transradial
- K180081 — RAILWAY Sheathless Access System
- K143412 — ADROIT Guiding Catheter
- K133843 — SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER
- K121442 — POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER
- K041796 — PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
- K034050 — CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F
Data sourced from openFDA. This site is unofficial and independent of the FDA.