14 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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KMA FLOW DIRECTED THERMODILUTION CATHETE
FDA 510(k)
FDA Class 2
·Cardiovascular
Polishers
FDA UDI
DFS - DIAMON GmbH·04057176151971·2comp pol. lense CA 6pcs
HEARTLINE RETRACTOR BLADES
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896095793·HEARTLINE RETRACTOR BLADES ATRIAL SOLID
ACUMED
FDA UDI
Acumed LLC·10806378045141·TRIAL Post-Lat Plates Bend Template
BIOSORBPDX BIOABSORBABLE FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Dental
MODIFICATION TO ENDOFAST RELIANT SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ACCU-CHEK ® PERFORMA TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·May 8, 2014
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·October 23, 2012
PFC CVD 10MM SZ3
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JWH·August 10, 2010
Exogen Express Bone Healing System, SAFHS, Part Numbers 71034200 and 71034140, Rx only, Smith & Nephew, 1450 Brooks Road, Memphis TX 38116. These are distributed internationally only. The device is used for the non-invasive treatment of established nonunions excluding skull and vertebra.
FDA Recall
Terminated
·Smith & Nephew Inc·Product code LPQ·June 5, 2009
Exogen 4000+ Ultrasound Bone Healing System, SAFHS, Part Numbers 71034100 and 71034101, Rx only, Smith & Nephew, 1450 Brooks Road, Memphis TX 38116. The device is used for the non-invasive treatment of established nonunions excluding skull and vertebra.
FDA Recall
Terminated
·Smith & Nephew Inc·Product code LPQ·June 5, 2009
Excelsior SL-10 Microcatheter, placed in sterile pouch. Manufactured by Boston Scientific Corporation, Fremont, CA. The ExcelsiorTM SL-10 Microcatheter is intended to assist in the delivery of diagnostic agents, such as contrast media, and therapeutic agents, such as occlusion coils, into the peripheral, coronary, and neurovasculature.
FDA Recall
Terminated
·Boston Scientific Corporation·Product code DQY·October 7, 2008
Jadak Barcode Scanner, Part No. 350587-32, 350587-41, 351377-32. Product Usage: An accessory for the Pyxis Anesthesia ES system and Pyxis Anesthesia system 4000 stations. The Jadak Barcode Scanner is used to scan medication labels during refill of the Pyxis Anesthesia ES system and Pyxis Anesthesia system 4000 stations and dispensing medication for patients.
FDA Recall
Terminated
·CareFusion 303, Inc.·Product code BRY·January 15, 2016
Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems
FDA Enforcement
Class II
·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021